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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833771Generated: November 1, 2026

Water → Ethyl 8-acetyl-12-hydroxy-12-methylheptadecanoate

https://huagongshe.com/reaction/1833771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54103623HCID 54103623—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductEthyl 8-acetyl-12-hydroxy-12-methylheptadecanoateHCID 20322206—

Reaction Steps

Mercuric acetate (3.8 g., 0.012 mole) is dissolved in water (12 ml.) and tetrahydrofuran (20 ml.) is added to give a suspension of a yellow solid. Then, ethyl 8-acetyl-12-methyl-11-heptadecenoate (4.2 g., 0.012 mole) in tetrahydrofuran (20 ml.) is added, and the mixture stirred at room temperature for 24 hours. After 6 hours, the yellow suspended solid has disappeared and a cloudy solution results. To the solution is added 3M sodium hydroxide solution (12 ml.), followed by 0.5M sodium borohydride solution in 3M sodium hydroxide (12 ml.). Liquids are decanted from the precipitated mercury. The organic layer is taken up in ether, washed with three portions of water and dried over sodium sulfate. Evaporation of the ether leaves 4.4 g. of ethyl 8-acetyl-12-hydroxy-12-methylheptadecanoate as a yellowish oil used in the next step without further purification; pmr (CDCl3) δ0.88 (3H,t), 1.13 (3H,s, CH3COH), 1.25 (3H,t, CH3CH2OCO-), 2.12 (3H,s, CH3CO), 4.12 (2H,q).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066692
Source datasetuspto-grants-1978_01
ORD IDord-0c1cfed80d354637be62094097341a20
Source noteuspto-grants-1978_01