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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974738Generated: October 29, 2026

Acetic Anhydride → HCID 53940283, compound

https://huagongshe.com/reaction/974738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHexaneHCID 8058—
Reactant2-DecenenitrileHCID 106459—
ReactantHCID 54322293HCID 54322293—
SolventPyridineHCID 1049—
ProductHCID 53940283HCID 53940283—

Reaction Steps

The pentadecadiene (D) (5.9 g) in 200 ml methanol containing eight drops concentrated HCl was refluxed for 15 minutes. After the solution was cooled, 400 ml of water were added, and the mixture was extracted three times with hexane. The hexane extract was dried over sodium sulfate, and the hexane was removed with a rotary evaporator leaving 3.1 g of crude 8,10-pentadecadienol, which was purified by silica gel liquid chromatography. Unwanted side products were eluted with 10% ether/hexane, and the alcohol was eluted with 50% ether/hexane, giving 2.5 g (66% yield based on the decenenitrile (B)). 8,10-Pentadecadienol in 75 ml pyridine and 5 ml acetic anhydride was refluxed 1.5 hours. After the solution was cooled, 200 ml hexane was added, and the mixture was extracted successively with water, 6N hydrochloric acid (twice), and water. The pentane phase was dried over sodium sulfate, filtered, and the pentane was removed by rotary evaporation, leaving crude product, which was purified by silica gel liquid chromatography (elution in 10% ether/hexane); the yield was 2.8 g (94% based on the alcohol). The product was 39% EE and 61% EZ by GC analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607670
Source datasetuspto-grants-1997_03
ORD IDord-1cc1d02ce4f34a81950025f262f9b1b9
Source noteuspto-grants-1997_03