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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905976Generated: October 30, 2026

HCID 13210860, compound → HCID 13210862, compound

https://huagongshe.com/reaction/1905976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13210860HCID 13210860—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductHCID 13210862HCID 1321086276%

Reaction Steps

The 1-benzyloxy-2-chloro-4-(2-phenethyloxyethoxy)-benzene obtained according to the preceding paragraph was stirred in 20 ml of 48% hydrogen bromide in glacial acetic acid at 25° C. for 30 minutes. The solution was evaporated to dryness and the residue was partitioned between 2N aqueous sodium hydroxide and diethyl ether. The aqueous phase was acidified to pH 6 with concentrated hydrochloric acid and extracted with ethyl acetate. The organic extract was washed with water, dried over sodium sulfate, filtered and evaporated to give 2.06 g (76%) of 2-chloro-4-(2-phenethyloxyethoxy)phenol in the form of an oil which was homogeneous according to chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04649160
Source datasetuspto-grants-1987_03
ORD IDord-9c42c10bba0144f7ae878233e3deb12e
Source noteuspto-grants-1987_03