Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

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Chemical Name:Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester
CAS No.:137653-88-4
Molecular Formula:C₃₁H₄₆O₈
Molecular Weight:546.701
Hs Code.:

Synonyms:Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

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Chemical Property of Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

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Technology Process of Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

There total 4 articles about Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl 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: 70.0%

: 98-88-4
benzoyl chloride

: 137653-87-3
(E)-(9R,12S,13R)-12,13-Diacetoxy-9-hydroxy-octadec-10-enoic acid ethyl ester

: 137653-88-4
Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

Guidance literature:: With pyridine; In dichloromethane; at 0 ℃; for 4h;
DOI:10.1016/S0040-4039(00)93494-4

Reference yield:

: 56703-12-9
8-Iodo-octanoic acid ethyl ester

: 137653-88-4
Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

2: 70 percent / pyridine / CH₂Cl₂ / 4 h / 0 °C

With pyridine; In dichloromethane;
DOI:10.1016/S0040-4039(00)93494-4

Reference yield:

: 17696-11-6
8-bromooctanoic acid

: 137653-88-4
Benzoic acid (E)-(1R,4S,5R)-4,5-diacetoxy-1-(7-ethoxycarbonyl-heptyl)-dec-2-enyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: NaI / acetone / 21 h / Heating

2: H₂SO₄ / 3 h / Heating

4: 70 percent / pyridine / CH₂Cl₂ / 4 h / 0 °C

With pyridine; sulfuric acid; sodium iodide; In dichloromethane; acetone;
DOI:10.1016/S0040-4039(00)93494-4