HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420580Generated: November 1, 2026
Ammonium formate → (S)-tert-Butyl 2-amino-3-hydroxypropanoate
https://huagongshe.com/reaction/1420580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N-(Benzyloxycarbonyl)-O-benzylserine, t-butyl ester | HCID 15778647 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-tert-Butyl 2-amino-3-hydroxypropanoate | HCID 11768865 | 99.6% |
Reaction Steps
A mixture of 29.24 g (0.076 mol) of (L) N-(benzyloxycarbonyl)-O-benzylserine, t-butyl ester from Reference Example 1, 24.1 g (0.38 mol) of ammonium formate and 38.3 g of 10% palladium on carbon in 600 ml of methanol was heated at 65° C. for 20 hours and stirred at room temperature overnight. The mixture was filtered through diatomaceous earth and the filter pad was washed with methanol. The filtrate was concentrated to give 12.18 g (99.6%) of product as described in Synthetic Commun., 26:2723 (1996).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06071903 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-a4502778dbda4127844521c2d8de52b5 |
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| Source note | uspto-grants-2000_06 |
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