Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823924Generated: October 30, 2026

Water → 4-tert-Butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid

https://huagongshe.com/reaction/1823924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
Reactant4-Tert-butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid methyl esterHCID 23570951—
SolventTetrahydrofuranHCID 8028—
Product4-tert-Butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acidHCID 2214795398%

Reaction Steps

To a solution of 4-tert-butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid methyl ester (12.3 g, 34 mmol) in THF (80 mL)/water (20 mL) was added lithium hydroxide (1.63 g, 68 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated and the residue diluted with water. After extraction with EtOAc, the aqueous phase was acidified to pH 5 by the addition of 2M aqueous hydrochloric acid solution. The aqueous phase was extracted with EtOAc and the extracts dried over magnesium sulfate. Concentration gave the title compound as a pale brown foam (11.54 g, 98%); 1H NMR (400 MHz, DMSO) δ 1.35 (9H, s), 1.74–1.81 (1H, m), 2.03–2.10 (1H, m), 2.81 (2H, m), 3.61 (1H, t), 6.86 (1H, m), 7.28 (1H, dd), 7.54 (1H, dd), 7.59 (1H, d), 12.60 (1H, brs); MS (ES−) m/e=346.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041687B2
Source datasetuspto-grants-2006_05
ORD IDord-abcf6e0a239345a1bae17a3dd71407b6
Source noteuspto-grants-2006_05