Category: 77186-95-9

77186-95-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Benzo[d]oxazol-2-ylmethanol, cas is 77186-95-9,the benzoxazole compound, it is a common compound, a new synthetic route is introduced below.

2.98 g (20.0 mmol) of 2-hydroxymethylbenzoxazole, 2.23 g (22.0 mmol) of triethylamine, 0.04 g (0.6 mmol) of 3,5-di-tert-butyl-4-hydroxytoluene were added to a 100 ml recovery flask. 2 mmol) and tetrahydrofuran 40 ml were added to prepare a reaction solution.After the reaction solution was cooled to 0 C., 2.30 g (22.0 mmol) of methacryloyl chloride was added dropwise and the mixture was stirred at room temperature for 3 hours, and the precipitated triethylamine hydrochloride was filtered off. Subsequently, the reaction solution was concentrated, and the extracting operation with 20 ml of ethyl acetate was carried out three times, and the extracted solutions were mixed and concentrated to obtain 4.09 g of a yellow liquid (yield: 94%).

The chemical industry reduces the impact on the environment during synthesis,77186-95-9,Benzo[d]oxazol-2-ylmethanol,I believe this compound will play a more active role in future production and life.

Reference：
Patent; SHIKOKU CHEMICALS CORPORATION; OKUMURA, NAOTO; IKEDA, YUICHI; (27 pag.)JP2015/20962; (2015); A;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem

Related Products of 77186-95-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.77186-95-9, Name is Benzo[d]oxazol-2-ylmethanol, molecular formula is C8H7NO2. In a article£¬once mentioned of 77186-95-9

Samarium Barbier reactions of alpha-iodomethyloxazoles and thiazoles with aliphatic aldehydes

(Chemical Equation Presented) The reductive coupling of substituted alpha-iodomethyloxazoles and thiazoles with aliphatic aldehydes under Barbier conditions provides an effective method for the direct incorporation of intact heterocyclic systems.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 77186-95-9

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

77186-95-9, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In a patent, 77186-95-9, molecular formula is C8H7NO2, introducing its new discovery.

BENZO AZOLE COMPOUND

PROBLEM TO BE SOLVED: To provide a novel benzo azole compound that is expected for use as material of light curable resin. SOLUTION: This invention relates to a benzo azole compound represented by formula (I) where R1 is a hydrogen atom or a methyl group, R2-R5 are a hydrogen atom, a C1-20 alkyl group, a halogen atom, a cyano group, a nitro group or the like, X is -NR6-, an oxygen atom or a sulfur atom, Y is -NR7- or an oxygen atom, R6-R7 are different or the same and a hydrogen atom, a C1-C20 alkyl group or the like, and n is an integer of 1-10. COPYRIGHT: (C)2015,JPO&INPIT

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.77186-95-9, you can also check out more blogs about77186-95-9

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

As a common heterocyclic compound, it belong benzoxazole compound,Benzo[d]oxazol-2-ylmethanol,77186-95-9,Molecular formula: C8H7NO2,mainly used in chemical industry, its synthesis route is as follows.,77186-95-9

2.98 g (20.0 mmol) of 2-hydroxymethylbenzoxazole, 2.23 g (22.0 mmol) of triethylamine, 0.04 g (0.6 mmol) of 3,5-di-tert-butyl-4-hydroxytoluene were added to a 100 ml recovery flask. 2 mmol) and tetrahydrofuran 40 ml were added to prepare a reaction solution.After the reaction solution was cooled to 0 C., 2.30 g (22.0 mmol) of methacryloyl chloride was added dropwise and the mixture was stirred at room temperature for 3 hours, and the precipitated triethylamine hydrochloride was filtered off. Subsequently, the reaction solution was concentrated, and the extracting operation with 20 ml of ethyl acetate was carried out three times, and the extracted solutions were mixed and concentrated to obtain 4.09 g of a yellow liquid (yield: 94%).

With the synthetic route has been constantly updated, we look forward to future research findings about Benzo[d]oxazol-2-ylmethanol,belong benzoxazole compound

Reference£º
Patent; SHIKOKU CHEMICALS CORPORATION; OKUMURA, NAOTO; IKEDA, YUICHI; (27 pag.)JP2015/20962; (2015); A;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem

77186-95-9, Benzo[d]oxazol-2-ylmethanol is a benzoxazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,77186-95-9

2.98 g (20.0 mmol) of 2-hydroxymethylbenzoxazole, 2.23 g (22.0 mmol) of triethylamine, 0.04 g (0.6 mmol) of 3,5-di-tert-butyl-4-hydroxytoluene were added to a 100 ml recovery flask. 2 mmol) and tetrahydrofuran 40 ml were added to prepare a reaction solution.After the reaction solution was cooled to 0 C., 2.30 g (22.0 mmol) of methacryloyl chloride was added dropwise and the mixture was stirred at room temperature for 3 hours, and the precipitated triethylamine hydrochloride was filtered off. Subsequently, the reaction solution was concentrated, and the extracting operation with 20 ml of ethyl acetate was carried out three times, and the extracted solutions were mixed and concentrated to obtain 4.09 g of a yellow liquid (yield: 94%).

As the paragraph descriping shows that 77186-95-9 is playing an increasingly important role.

Reference£º
Patent; SHIKOKU CHEMICALS CORPORATION; OKUMURA, NAOTO; IKEDA, YUICHI; (27 pag.)JP2015/20962; (2015); A;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem