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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154617Generated: October 31, 2026

Benzyl Alcohol → HCID 20434082, compound

https://huagongshe.com/reaction/1154617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13365127HCID 13365127—
Reactantalpha-(alpha-Methyl-4-methoxyphenethylimino)-2-methoxyacetophenoneHCID 20434109—
SolventEthanolHCID 702—
ProductHCID 20434082HCID 20434082—

Reaction Steps

A mixture of the α-(α-methyl-4-methoxyphenethylimino)-2-methoxyacetophenone solution, 0.76 g of sodium borohydride and 12 ml of ethanol is treated in the same manner as described in Example 1-(3), whereby α-[(α-methyl-4-methoxyphenethylamino)methyl]-2-methoxybenzylalcohol [the mixture of two diastereoisomers] is obtained as a crude oil. Said benzylalcohol [i.e., the mixture of two diastereoisomers] is treated with ethanolic hydrogen chloride to convert it into its hydrochloride, and the hydrochloride is recrystallized from a mixture of ethanol and ether. The crystalline precipitates are collected by filtration (the filtrate is hereinafter referred to as "mother liquor"). 1.85 g of α-[(α-methyl-4-methoxyphenethylamino)methyl]-2-methoxybenzylalcohol hydrochloride [the diastereoisomer of M.p. 161°-163° C.] is thereby obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490392
Source datasetuspto-grants-1984_12
ORD IDord-0f0b46c074a44686bb6cef8e47fd2df2
Source noteuspto-grants-1984_12