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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846552Generated: October 30, 2026

Bromhydrol → HCID 14716731, compound

https://huagongshe.com/reaction/846552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromhydrolHCID 166749—
ReactantHCID 54436508HCID 54436508—
SolventTolueneHCID 1140—
ProductHCID 14716731HCID 1471673198%

Reaction Steps

Into a flask of 50 m were charged 1.84 g (7.4 mmol) of 4-(2-methyloctanoyl) anisole and 35 ml of dried toluene, to which was added 8.68 g of anhydrous aluminum bromide under ice cooling with stirring, and further the stirring was continued at room temperature over a night. Thereafter, the reaction mixture was stirred at 40° C. for 4 hours, cooled to room temperature and poured into 100 ml of ice water. After the extraction with 40 ml of toluene twice, the organic layer was washed with 80 ml of water, dried on magnesium sulfate, filtered, concentrated and distilled under a reduced pressure to obtain 1.70 g (7.3 mmol, yield 98%) of a redish brown and oily (+)-4-(2-methyloctanoyl) phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137653
Source datasetuspto-grants-1992_08
ORD IDord-31761682302749f1a40436eb714e2c60
Source noteuspto-grants-1992_08