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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509511Generated: November 4, 2026

HCID 68731586, compound → HCID 68732363, compound

https://huagongshe.com/reaction/509511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68731586HCID 68731586—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 68732363HCID 6873236384%

Reaction Steps

A mixture of 4-(tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid (56.57, 190.9 mmol) in methanol (250 mL) and palladium/carbon (5.66 g, 10% weight) 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 brown oil, which was stirred in ether (300 mL) overnight. The ether slurry was filtered to give 2-amino-4-(tert-butoxycarbonylamino-methyl)-benzoic acid as a brown solid (42.0 g, 84% yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096573B2
Source datasetuspto-grants-2015_08
ORD IDord-48fe4c0c320b4262a0dcc177e8636036
Source noteuspto-grants-2015_08