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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386103Generated: October 31, 2026

HCID 68637842, compound → HCID 86595374, compound

https://huagongshe.com/reaction/2386103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68637842HCID 68637842—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 86595374HCID 86595374—

Reaction Steps

PCC (9.7 g, 45 mmol) was added in portions to a solution containing 6-benzyloxy-1-tetradecanol (7.5 g, 30 mmol) in methylene chloride (100 ml) at RT. The black mixture was stirred for 2 hours, then filtered through a bed of silica gel using hexane:ethyl acetate (90:10). The corresponding aldehyde, 6-benzyloxy-tetradecanal, was produced at a yield of 6.1 g (81%). This aldehyde compound was mixed with carbethoxymethylene triphenylphosphorane (10 g, 29 mmol) in 100 ml of methylene chloride at RT. The mixture was allowed to stir overnight, after which the solvent was removed and replaced with hexane. Solid precipitates were removed by filtration. Following chromatography on silica gel using hexane:ethyl acetate at a ratio of 90:10, the corresponding ester was detected at 8.4 g scale (90%). The chemical shift of the ester, 8-benzyloxyhexadec-2-enoate ethyl ester, is as follows: 1H-NMR (CDCl3) δ 0.89 (m, 6H, CH3), 1.2-1.5 (m, 20H, CH2), 2.2 (m, 2H, CH2—C═), 3.35 (m, 2H, CH2O), 4.2 (q, 2H, MeCH2—O), 4.55 (dd, 2H, CH2—O), 5.8 (d, 1H, CH═C), 6.95 (d, t 1H, CH═C), 7.35 (m, 5H, benzyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268291B2
Source datasetuspto-grants-2012_09
ORD IDord-de9a1b300ab3485ab9085b7ba00b89dd
Source noteuspto-grants-2012_09