HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452539Generated: October 29, 2026
HCID 67363471, compound → HCID 67364561, compound
https://huagongshe.com/reaction/452539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67363471 | HCID 67363471 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67364561 | HCID 67364561 | 95.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492376B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-710fc37983d944a484caad0a83a16d71 |
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| Source note | uspto-grants-2013_07 |
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