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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573517Generated: October 31, 2026

Sodium Hydroxide → (2R)-2-{[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]methyl}oxirane

https://huagongshe.com/reaction/573517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(+)-EpichlorohydrinHCID 149428—
ReactantLinoleyl alcoholHCID 5365682—
CatalystTetrabutylammonium BromideHCID 74236—
SolventHexaneHCID 8058—
Product(2R)-2-{[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]methyl}oxiraneHCID 58434808—

Reaction Steps

A 250 mL rb flask was charged with magnetic stirbar, tetrabutyl ammonium bromide (TBAB, 2.72 g, 8.4 mmol), linoleyl alcohol (225 g, 884 mmol), and sodium hydroxide (50.7 g, 1.2 mol), then cooled in an ice bath. The (S)-epichlorohydrin (156 g, 1.69 mol) was added slowly over 2 hours and then warmed to ambient temperature and stirred overnight. 259 mL of hexane was added and allowed to stir for 15 mins, then mixture was filtered and organic layer was concentrated in vacuo. The product was purified using 0-10% ethyl acetate/hexane gradient on 330 g silica column to give (2R)-2-{[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]methyl}oxirane. 1H NMR (CDCl3, 300 mHz) δ 0.90-0.86 (m, 3H), 1.29 (s, 16H), 1.55-1.64 (m, 2H), 2.00-2.07 (m, 4H), 2.58-2.61 (m, 1H), 2.74-2.80 (m, 3H), 3.12-3.15 (m, 1H) 3.34-3.52 (m, 3H), 3.67-3.72 (dd, J=12 Hz, 1H) 5.30-5.35 (m, 4H); HRMS (m+1) calcd 323.2872. Found 323.2951.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029604B2
Source datasetuspto-grants-2015_05
ORD IDord-04ee70d0c608468d9f1dc110fcf30602
Source noteuspto-grants-2015_05