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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262604Generated: October 31, 2026

4-Methoxyphenol → HCID 13320244, compound

https://huagongshe.com/reaction/1262604

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
Reactant3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexaneHCID 9815370—
CatalystWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13320244HCID 13320244—

Reaction Steps

A mixture of 17.5 g. (0.10 mole) of 1-benzyl-3,4-epoxypyrrolidine, 13.4 g. (0.11 mole) of p-methoxyphenol, and 3 drops of water was heated on a steam bath overnight. The dark residue was dissolved in methylene chloride and the solution was washed with two 50-ml. portions of 5% sodium hydroxide. The methylene chloride layer was dried over anhydrous sodium sulfate and concentrated to give 23.7 g. of viscous dark oil. This oil was chromatographed on 480 g. of silica gel 60 and the product was eluted with a 1:1 benzene:ether solution. The appropriate fractions were concentrated to give 10.0 g. of a yellow oil which crystallized upon scratching. The solid was recrystallized from cyclohexane to yield 7.2 g. (24%) tan solid, m.p. 84°-5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452809
Source datasetuspto-grants-1984_06
ORD IDord-272d87270ec54ba5bc1b8cdfa9ff9101
Source noteuspto-grants-1984_06