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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823643Generated: October 30, 2026

Allyl Alcohol → HCID 11426846, compound

https://huagongshe.com/reaction/1823643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantHCID 11196464HCID 11196464—
SolventDichloromethaneHCID 6344—
ProductHCID 11426846HCID 11426846—

Reaction Steps

(1S,2S,5R,6S)-2-Allyloxycarbonylamino-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid (13.4 g, 49.81 mmol, 1.0 equiv) was suspended in methylene chloride (400 mL). N-Ethyl-N′-dimethylaminopropylcarbodiimide (9.55 g, 49.81 mmol, 1.0 equiv) and dimethylaminopyridine (0.608 g, 4.98 mmol, 0.1 equiv) were added at room temperature under nitrogen. After a solution formed, allyl alcohol (3.4 mL, 2.89 g, 49.81 mmol, 1.0 equiv) was added and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with methylene chloride and washed twice with water. The organic phase was dried over magnesium sulfate, filtered and concentrated. The title compound was obtained as an oil (44% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07038077B2
Source datasetuspto-grants-2006_05
ORD IDord-018d42a32d5b4eefb332170afb56ccb9
Source noteuspto-grants-2006_05