HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445761Generated: November 2, 2026
Acetone → 4-Benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acid
https://huagongshe.com/reaction/1445761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-2-fluorobenzoyl chloride | HCID 2734026 | — |
| Reactant | 2-Amino-4-(benzyloxy)butanoic acid hydrochloride | HCID 68698920 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | 4-Benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acid | HCID 58951433 | — |
Reaction Steps
To a stirring solution of 2-amino-4-benzyloxy-butyric acid hydrochloride salt (1.0 mmol) (See Intermediate 34) and sodium carbonate (3.0 mmol) in 1:1 acetone/water (0.5M) in a 0° C. ice bath, slowly add 4-bromo-2-fluoro-benzoyl chloride (1.2 mmol) diluted in acetone (prepared from 4-bromo-2-fluoro-benzoic acid (1.0 mmol) and oxalyl chloride (1.0 mmol) in dichloromethane using catalytic dimethylformamide). Stir for 30 minutes at 0° C. After this time, wash the reaction with 1N hydrochloric acid while extracting with ethyl acetate. Concentrate the organics in vacuo. Purify on an Isco CombiFlash® chromatography system eluting with 1% acetic acid in ethyl acetate and hexane. MS (m/e) (79Br/81Br): 410.3/412.3 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666871B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-abf392cb93b945ac93ee06688db8ca0d |
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| Source note | uspto-grants-2010_02 |
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