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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751946Generated: October 28, 2026

Water → HCID 13736245, compound

https://huagongshe.com/reaction/1751946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantHexaneHCID 8058—
ReactantTriethylamineHCID 8471—
SolventDimethylacetamideHCID 31374—
ProductHCID 13736245HCID 1373624554%

Reaction Conditions

Temperature117.5 °C

Reaction Steps

(2E)-4-Methylhepta-2,6-dienoic acid (67.74 g) obtained by the method described above was dissolved in N,N-dimethylacetamide (210 mL) under a nitrogen atmosphere. To the solution, acetic anhydride (91 mL, 0.96 mol) and triethylamine (67 mL, 0.48 mol) were added. The reaction mixture was warmed and stirred at 115 to 120° C. for 6 hours. The reaction mixture was cooled to room temperature, and n-hexane (360 mL) and water (540 mL) were added thereto to separate an organic layer. The aqueous layer was subjected to two extractions with hexane (each with 180 mL), and all the organic layers were combined and then washed with a 5% aqueous sodium bicarbonate solution (90 mL) and water (90 mL) in this order. The obtained organic layer was concentrated under reduced pressure, and the residue was distilled (74-76° C., approximately 25 mmHg) to obtain the title compound (39.09 g, colorless oil substance) (overall yield from 1,1-bis(allyloxy)propane: 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162971B2
Source datasetuspto-grants-2015_10
ORD IDord-698137a18f3149f38efe30336d6fcb6d
Source noteuspto-grants-2015_10