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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372897Generated: October 29, 2026

Sodium Hydroxide → Ethyl 8-acetyl-12-hydroxy-12-methylheptadecanoate

https://huagongshe.com/reaction/372897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54103623HCID 54103623—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
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 is 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) δ 0.88 (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 numberUS04092356
Source datasetuspto-grants-1978_05
ORD IDord-6e553390d5e141868426a7068e310da1
Source noteuspto-grants-1978_05