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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381228Generated: November 2, 2026

4-Methoxyphenol → HCID 13320244, compound

https://huagongshe.com/reaction/1381228

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 numberUS04585785
Source datasetuspto-grants-1986_04
ORD IDord-1bdc119089be46b5bd675fa0b9449bd9
Source noteuspto-grants-1986_04