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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972132Generated: November 3, 2026

Triethylamine → HCID 20396662, compound

https://huagongshe.com/reaction/972132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 20396656HCID 20396656—
ReactantHCID 21822430HCID 21822430—
SolventO-XyleneHCID 7237—
ProductHCID 20396662HCID 20396662—

Reaction Steps

4-(2,2-Dimethoxyethoxy)phenol (0.05 mole), N-allyl-N-benzylcarbamoyl chloride (0.08 mole), triethylamine (0.05 mole) and xylene (50 ml) are charged into a glass reaction flask equipped with a mechanical stirrer, thermometer and reflux condenser. The mixture is stirred and heated at reflux for a period of about 12 hours. After this time the reaction mixture is cooled to room temperature and is filtered. The filtrate is then washed with water and dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent and unreacted starting materials to yield the desired product O-[4-(2,2-dimethoxyethoxy)phenyl] N-allyl-N-benzylcarbamate as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163112
Source datasetuspto-grants-1979_07
ORD IDord-7d2d49d39e014b5c82f72a55f4407e0b
Source noteuspto-grants-1979_07