Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

Base Information

Chemical Name:Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester
CAS No.:306726-12-5
Molecular Formula:C₃₆H₄₁NO₅SSi
Molecular Weight:627.877
Hs Code.:

Synonyms:Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

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Chemical Property of Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

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Technology Process of Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

There total 5 articles about Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-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: 98.0%

: 98-88-4
benzoyl chloride

: 306726-10-3
(1R,2S,3S)-2,3-Bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butan-1-ol

: 306726-12-5
Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 25 ℃; for 2h;
DOI:10.1002/(SICI)1521-3773(19991115)38:22<3340::AID-ANIE3340>3.0.CO;2-2

Reference yield:

: 65973-56-0
(S,S)-2,3-bis-allyloxy-butane-1,4-diol

: 306726-12-5
Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 90 percent / NaH; Bu₄NI / tetrahydrofuran / 4 h / 0 - 25 °C

2.1: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / 4 h / -78 - -40 °C

3.1: TMS / -40 - 0 °C

3.2: PPTS; MeOH / 0 - 25 °C

4.1: 98 percent / Et₃N; 4-DMAP / CH₂Cl₂ / 2 h / 0 - 25 °C

With dmap; oxalyl dichloride; tetramethylsilane; tetra-(n-butyl)ammonium iodide; sodium hydride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; 1.1: Etherification / 2.1: Oxidation / 3.1: Addition / 3.2: Solvolysis / 4.1: Esterification;
DOI:10.1002/(SICI)1521-3773(19991115)38:22<3340::AID-ANIE3340>3.0.CO;2-2

Reference yield:

: 65973-54-8
(2R,3R)-2,3-Bis-allyloxy-succinic acid diethyl ester

: 306726-12-5
Benzoic acid (1R,2R,3S)-2,3-bis-allyloxy-4-(tert-butyl-diphenyl-silanyloxy)-1-thiazol-2-yl-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 93 percent / LAH / diethyl ether / 25 - 35 °C

2.1: 90 percent / NaH; Bu₄NI / tetrahydrofuran / 4 h / 0 - 25 °C

3.1: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / 4 h / -78 - -40 °C

4.1: TMS / -40 - 0 °C

4.2: PPTS; MeOH / 0 - 25 °C

5.1: 98 percent / Et₃N; 4-DMAP / CH₂Cl₂ / 2 h / 0 - 25 °C

With dmap; lithium aluminium tetrahydride; oxalyl dichloride; tetramethylsilane; tetra-(n-butyl)ammonium iodide; sodium hydride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; 1.1: Reduction / 2.1: Etherification / 3.1: Oxidation / 4.1: Addition / 4.2: Solvolysis / 5.1: Esterification;
DOI:10.1002/(SICI)1521-3773(19991115)38:22<3340::AID-ANIE3340>3.0.CO;2-2