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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065735Generated: October 30, 2026

Sodium Thiosulfate → HCID 68606931, compound

https://huagongshe.com/reaction/2065735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 68606931HCID 6860693128%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-amino-2-chloro-benzoic acid methyl ester (6.76 g, 36.4 mmol) in dichloromethane (100 mL) and methanol (50 mL) was added tetra-n-butylammonium tribromide (17.7 g, 36.4 mmol). The mixture was stirred at 25° C. for 90 minutes. Sodium thiosulfate (10% aqueous solution) was added and the mixture was extracted with dichloromethane. The combined extracts were washed with water, dried (Na2SO4), filtered, and concentrated to dryness under reduced pressure. The crude material was purified by flash column chromatography (hexane/acetone 8:2). Fractions with the desired product were concentrated to small volume. The resulting suspension was allowed to stand for two hours and was then filtered to obtain 5-amino-6-bromo-2-chloro-benzoic acid methyl ester as a white solid (2.7 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288552B2
Source datasetuspto-grants-2012_10
ORD IDord-019d505be7c3401e86ca3cc3e505a230
Source noteuspto-grants-2012_10