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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283439Generated: October 30, 2026

Acetic Acid → HCID 89545047, compound

https://huagongshe.com/reaction/2283439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantButanoic acid, 3-aMino-, ethyl ester, hydrochloride, (3S)-HCID 42614517—
ReactantHCID 89544754HCID 89544754—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 89545047HCID 8954504741.6%

Reaction Steps

Step 1 To a solution of 3-benzoyl-4-chloro-2-fluoro-benzaldehyde (Intermediate 10, 337 mg, 1.29 mmol) in dichloroethane (5 ml) was sequentially added (S)-3-amino-butyric acid ethyl ester hydrochloride (237 mg, 1.41 mmol), triethylamine (0.196 ml, 1.41 mmol), sodium triacetoxyborohydride (818 mg, 3.86 mmol) and glacial acetic acid (0.159 ml 2.57 mmol). The mixture was stirred for 2 days then dilute sodium bicarbonate was added. After stirring for 10 minutes, the mixture was extracted with ethyl acetate. The organic liquors were washed with water and brine, dried (MgSO4) and concentrated. The residue was purified by silica chromatography eluting with 20-100% ethyl acetate/petroleum ether furnishing (3S)-3-(3-benzoyl-4-chloro-2-fluoro-benzylamino)-butyric acid ethyl ester as a colourless oil (203 mg). MS: [M+H] 378

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145354B2
Source datasetuspto-grants-2015_09
ORD IDord-a0064b92e7794a21989a6ec430afecfc
Source noteuspto-grants-2015_09