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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091435Generated: November 2, 2026

Acetic Acid → HCID 57725383, compound

https://huagongshe.com/reaction/1091435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 66593713HCID 66593713—
SolventTrimethyl orthoformateHCID 9005—
ProductHCID 57725383HCID 5772538342%

Reaction Steps

2-(2-amino-5-chloro-benzoylamino)-butyric acid-tert-butyl ester (2.82 g) was dissolved in trimethylorthoformate (50 ml). Acetic acid (10 ml) was added, and reaction mixture refluxed for 48 hours. After this time, the solvents were removed and the residue partitioned between ethyl acetate and saturated sodium bicarbonate solution. The aqueous layer was further extracted with ethyl acetate and the combined organic extracts washed with brine, dried (MgSO4) and concentrated under reduced pressure to give a yellow oil. This was purified by flash chromatography (20% EtOAc: Petroleum) to give the sub-title compound as an oil (1.23 g, 42% yield). 1H NMR (400 MHz, CDCl3) δ 8.25 (1H, s), 8.05 (1H, s), 7.7 (2H, m), 5.3 (1H, m), 2.3 (1H, m), 2.0 (1H, m), 1.5 (9H, s), 1.0 (3H, t) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129381B2
Source datasetuspto-grants-2012_03
ORD IDord-3cc630935930483d92e2ad72f70d0e5b
Source noteuspto-grants-2012_03