Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372283Generated: October 30, 2026

Methyl iodide → trans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamide

https://huagongshe.com/reaction/372283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN-(4-Oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetamideHCID 13037024—
CatalystSilver(II) oxideHCID 92152—
SolventTetrahydrofuranHCID 8028—
Producttrans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamideHCID 70617063—

Reaction Steps

A mixture of racemic N-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)acetamide (3.9 g) and 150 ml. tetrahydrofuran (THF) is stirred and 17 ml. of methyl iodide and 24.4 g. of freshly prepared silver oxide are added over a 4-hour period, under a nitrogen atmosphere. After 16 hours, an additional 10 ml. of methyl iodide and 11.4 g. of silver oxide are added over a 4-hour period and stirring is continued for 2 days. The mixture is filtered through a layer of celite and the filter cake washed with THF (2 × 75 ml.). The filtrate and wash solution are combined and evaporated to dryness in vacuo to afford 4.3 g. of solid. The solid is recrystallized from hexane/ether to afford 2.4 g. of title compound, melting point 97°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04089976
Source datasetuspto-grants-1978_05
ORD IDord-ee56eb2cb536446aa3b424cafc4775cb
Source noteuspto-grants-1978_05