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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616213Generated: October 29, 2026

HCID 20371721, compound → HCID 20371608, compound

https://huagongshe.com/reaction/616213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20371721HCID 20371721—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
ProductHCID 20371608HCID 20371608—

Reaction Steps

A mixture of 3-(4-nitrobenzamido)-4-hydroxy-α-(tert.butylaminomethyl)benzylalcohol hydrochloride (7.37 g, 0.018 mole), PtO2 (250 mg), and methanol (225 ml) was placed in a pressure hydrogenation apparatus at a starting pressure of 2 atm. The hydrogenation was started, and the calculated amount of hydrogen was taken up within 17 minutes. The hydrogenation was interrupted and the platinum catalyst was filtered off. The clear colorless filtrate was evaporated on a rotary evaporator at 40° - 50° C. The residue, a cream-colored foam (7.3 g), was recrystallized three times from methanol/ether, and 3.50 g (50%), m.p. 228.8° - 230° C, of analytically pure 3-(4-aminobenzamido)-4-hydroxy-α-(tert.butylaminomethyl)benzylalcohol hydrochloride, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072760
Source datasetuspto-grants-1978_02
ORD IDord-56b7f56aae0d4cc6afcd2e75011e23e2
Source noteuspto-grants-1978_02