HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989152Generated: October 29, 2026
Ammonium formate → Methyl 2-amino-2-(4-fluorophenyl)acetate
https://huagongshe.com/reaction/989152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-Fluoro-alpha-[(phenylmethyl)amino]benzeneacetic acid methyl ester hydrochloride | HCID 69360922 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methyl 2-amino-2-(4-fluorophenyl)acetate | HCID 10943118 | 87% |
Reaction Steps
4-Fluoro-α-[(phenylmethyl)amino]benzeneacetic acid methyl ester hydrochloride (12.2 kg, 39.4 moles) was added to a slurry of 10% palladium-on-carbon (1.2 kg) in isopropanol (50 L). Ammonium formate (5.0 kg, 79.4 moles) was added and the batch was heated to 50° C. Progress of the reaction was monitored by HPLC. The batch was filtered through Hyflo Supercel and the filter cake was washed with isopropanol (25 L). The filtrate was evaporated to low volume and flushed with isopropyl acetate (50 L). The residue was dissolved in isopropyl acetate (30 L) and washed with 5% aqueous potassium phosphate (40 L), followed by saturated aqueous sodium chloride (10 L). The solution was evaporated under vacuum to give 5.79 kg (87% yield) of racemic α-amino-4-fluorobenzeneacetic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638930B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-7a3583cc1ba04560993a9425131dc961 |
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| Source note | uspto-grants-2003_10 |
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