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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049986Generated: October 29, 2026

Water → (E,E,E)-7-benzylcarbamoyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol

https://huagongshe.com/reaction/2049986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzylamineHCID 7504—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(E,E,E)-7-carboxy-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-olHCID 12084974—
SolventDichloromethaneHCID 6344—
Product(E,E,E)-7-benzylcarbamoyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-olHCID 70588013—

Reaction Conditions

Temperature0 °C

Reaction Steps

660 mg of (E,Z,E) and (E,E,E)-7-carboxy-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol was dissolved in 10 ml of dichloromethane. The solution was cooled to 0° C., 440 mg of dicyclohexylcarbodiimide was added and the mixture was stirred for 1 hour. Then, 0.5 ml of benzylamine was added and stirring was continued for 1 hour. The reaction mixture was left at room temperature overnight and water was added followed by extraction with ethyl ether. The oily substance derived from the extract was purified by a thin-layer chromatography to afford 315 mg of the end product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04199519
Source datasetuspto-grants-1980_04
ORD IDord-0ffb88ad90e741cbb602fa878b963f9c
Source noteuspto-grants-1980_04