HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616213Generated: October 29, 2026
HCID 20371721, compound → HCID 20371608, compound
https://huagongshe.com/reaction/616213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20371721 | HCID 20371721 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20371608 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04072760 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-56b7f56aae0d4cc6afcd2e75011e23e2 |
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| Source note | uspto-grants-1978_02 |
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