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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868254Generated: November 2, 2026

HCID 66642923, compound → HCID 66643161, compound

https://huagongshe.com/reaction/1868254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66642923HCID 66642923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 66643161HCID 6664316165.1%

Reaction Steps

A mixture of 2-(tert-butoxycarbonylamino-methyl)-6-nitro-benzoic acid (2.19 g, 75 mmol) in methanol (530 mL) and palladium/carbon (0.2 g) was hydrogenated with a Parr-shaker overnight at 51 psi. The black mixture was filtered through a pad of Celite, and the filtrate was evaporated to give a foamy brown oil, which was stirred in ether (300 mL) overnight. The suspension was filtered to give 2-amino-6-(tert-butoxycarbonylamino-methyl)-benzoic acid as a yellow solid (13.0 g, 65% yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635700B2
Source datasetuspto-grants-2009_12
ORD IDord-99ea7177c7724eba8cb4199d904fcf8b
Source noteuspto-grants-2009_12