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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41724Generated: October 25, 2026

Ethyl Acetate → HCID 86660475, compound

https://huagongshe.com/reaction/41724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLinoleoyl chlorideHCID 9817754—
ReactantHCID 86660473HCID 86660473—
SolventPyridineHCID 1049—
ProductHCID 86660475HCID 8666047565%

Reaction Conditions

Temperature50 °C

Reaction Steps

Linoleoyl chloride (208 mg, 0.696 mmol) was added to a solution of (E)-3-(3′-adamantan-1-yl-4′-hydroxybiphenyl-4-yl)-acrylic acid tert-butyl ester (200 mg, 0.464 mmol) in pyridine (2.2 ml). The resulting mixture was heated to 50° C. for 1 h, and then stirred at RT overnight. After addition of EtOAc, the organic phase was washed twice with 1N HCl, water, dried over Na2SO4, filtered and removed under reduced pressure. (E)-Octadeca-9,12-dienoic acid 3-adamantan-1-yl-4′-(2-tert-butoxycarbonylvinyl)biphenyl-4-yl ester was obtained as a colourless oil after purification on silica gel (EtOAc/hexane 5:95) in 65% yield (210 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530517B2
Source datasetuspto-grants-2013_09
ORD IDord-470bff9b5847421b9928813953b96742
Source noteuspto-grants-2013_09