(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester
CAS No.:914643-61-1
Molecular Formula:C₁₇H₂₁NO₂S
Molecular Weight:303.425
Hs Code.:

Synonyms:(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Suppliers and Price of (R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of (R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

There total 3 articles about (R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 68.0%

: 2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

: 106-95-6
allyl bromide

: 914643-61-1
(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Guidance literature:: With potassium hydroxide; binaphthalenyl-based chiral ammonium base bromide; In toluene; at 0 ℃; for 0.5h;
DOI:10.1021/jo061107t

Reference yield:

: 3113-46-0,18711-91-6,2518-12-9
2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid methyl ester

: 914643-61-1
(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / trimethylaluminum / toluene / 96 h / Heating

2: 68 percent / binaphthalenyl-based chiral ammonium base bromide; KOH / toluene / 0.5 h / 0 °C

With potassium hydroxide; binaphthalenyl-based chiral ammonium base bromide; trimethylaluminum; In toluene;
DOI:10.1021/jo061107t

Reference yield:

: 5873-90-5
methyl benzimidate hydrochloride

: 914643-61-1
(R)-4-allyl-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / triethylamine / CH₂Cl₂ / 6 h / Heating

2: 90 percent / trimethylaluminum / toluene / 96 h / Heating

3: 68 percent / binaphthalenyl-based chiral ammonium base bromide; KOH / toluene / 0.5 h / 0 °C

With potassium hydroxide; binaphthalenyl-based chiral ammonium base bromide; trimethylaluminum; triethylamine; In dichloromethane; toluene;
DOI:10.1021/jo061107t