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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210276Generated: November 1, 2026

HCID 10946429, compound → HCID 11077426, compound

https://huagongshe.com/reaction/2210276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10946429HCID 10946429—
SolventMethanolHCID 887—
ProductHCID 11077426HCID 1107742613.1%

Reaction Steps

A 500 ml autoclave was loaded in a glove box with 15.0 g (50.4 mmol) of (Z)-2-acetyl-1-(p-methoxybenzylidene)-1,2,3,4,5,6,7,8-octahydroisoquinoline, 170 ml of methanol and the catalyst solution prepared according to a). The hydrogenation was carried out at 100° and 35 bar for 22 hours. The conversion was 98.5%. A 2 g product-containing aliquot of the hydrogenation solution was evaporated and the residue was dissolved in diethyl ether. The ether solution was filtered through a silica gel pad in order to separate the catalyst. Evaporation of the filtrate gave 1.97 g of (S)-2-acetyl-1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline as yellowish crystals of 95.9% e.e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457219
Source datasetuspto-grants-1995_10
ORD IDord-3ec6439ff4d745f5ac1c3e277e79fb6f
Source noteuspto-grants-1995_10