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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446752Generated: October 29, 2026

HCID 67363471, compound → HCID 67364561, compound

https://huagongshe.com/reaction/446752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67363471HCID 67363471—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystZinc bromideHCID 10421208—
SolventEthyl AcetateHCID 8857—
ProductHCID 67364561HCID 6736456195.5%

Reaction Steps

To a solution of [tert-butoxycarbonyl-(5-chloro-2-nitro-benzyl)-amino]-acetic acid ethyl ester (69.0 g, 0.186 mol) in ethyl acetate (1200 ml) was added zinc bromide (8.5 g, 0.037 mol). The reaction mixture was purged with argon after 15 minutes. After addition of the palladium catalyst (10% on activated charcoal, 7.9 g, 0.0074 mol) the mixture was hydrogenated at ambient pressure during a period of ca. 48 h until ca. 13 l of hydrogen gas had been consumed. The catalyst was removed by filtration and the filtrate was washed with two portions of saturated aqueous sodium bicarbonate solution and brine, each. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound (60.6 g, 95.5%) as yellow waxy solid. MS m/e: 343 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481528B2
Source datasetuspto-grants-2013_07
ORD IDord-43b9ccb50ec1484cbd14a66843e34205
Source noteuspto-grants-2013_07