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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719817Generated: November 3, 2026

Acetic Acid → 1-(3-Phenoxyphenyl)propan-1-ol

https://huagongshe.com/reaction/1719817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-PhenoxybenzaldehydeHCID 38284—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Phenoxyphenyl)propan-1-olHCID 15185477—

Reaction Steps

A mixture of 25.1 g of 3-phenoxybenzaldehyde in 23 ml of an anhydrous tetrahydrofuran is added dropwise to 60 ml of 3-N-ethylmagnesium bromide in ethyl ether, cooled in an ice bath under a nitrogen atmosphere, over a period of about 1 1/2 hours. The reaction mixture is stirred overnight and warmed to room temperature, after which time it is poured over ice containing 12 ml of acetic acid. The organic and aqueous phases are separated and the aqueous phases extracted twice with ethyl ether. The ethereal extracts are combined and washed with a solution prepared from 3 g of sodium carbonate and 40 ml of water. The aqueous wash layers are extracted further with ethyl ether and the combined ethereal extracts are dried over anhydrous sodium sulfate and filtered. The ether is removed under reduced pressure to yield 29.45 g of 1-(3-phenoxyphenyl)propan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542237
Source datasetuspto-grants-1985_09
ORD IDord-cab4282edf7c40988ed7ac062cdaa457
Source noteuspto-grants-1985_09