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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451682Generated: October 30, 2026

Allyl bromide → HCID 19702682, compound

https://huagongshe.com/reaction/1451682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant3-(Methylamino)phenolHCID 10820513—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 19702682HCID 19702682137.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 3-(N-methylamino)phenol (10 g, 80 mmol), dissolved in 80 ml of NMP, was added allyl bromide (9.8 ml, 113 mmol) via syringe. The yellow solution was heated to 80° C. for 4 hours. The reaction mixture was poured into distilled water (200 ml) and saturated aqueous sodium bicarbonate solution was added. Extraction with diethyl ether (3×200 ml), drying over anhydrous magnesium sulfate, filtration and concentration in vacuo yielded 18.0 g of 3-(N-allyl-N-methylamino)phenol as a viscous green tinted oil. Vacuum distillation at I torr (110°-120° C.) yielded 10.5 g (80%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605726
Source datasetuspto-grants-1997_02
ORD IDord-6aa1310933884ed7be6456fd3c7ad7a8
Source noteuspto-grants-1997_02