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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596604Generated: November 4, 2026

Methanol → 2(S)-amino-3(R)-(4-iodophenyl)-butyric acid, methyl ester hydrochloride

https://huagongshe.com/reaction/1596604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2(S)-amino-3(R)-(4-iodophenyl)-butyric acidHCID 54216241—
Product2(S)-amino-3(R)-(4-iodophenyl)-butyric acid, methyl ester hydrochlorideHCID 8675740082%

Reaction Steps

To an ice cooled solution of 2(S)-amino-3(R)-(4-iodophenyl)-butyric acid (124 mg, 0.42 mmol) in methanol (0.5 mL) was added dropwise thionyl chloride (150 μL, 2.0 mmol). Methanol (1 mL) was added and the reaction mixture was heated to reflux for 2 hr. After cooling, the mixture was filtered and the filtrate concentrated by rotoevaporation to yield 2(S)-amino-3(R)-(4-iodophenyl)-butyric acid, methyl ester hydrochloride (116 mg, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291511B1
Source datasetuspto-grants-2001_09
ORD IDord-64c0aafae0dc4312a4fc7df6d0a34bf1
Source noteuspto-grants-2001_09