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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646134Generated: October 29, 2026

Sulfuryl chloride → ethyl 5-bromo-3-chloro-1H-indole-2-carboxylate

https://huagongshe.com/reaction/646134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantEthyl 5-Bromoindole-2-carboxylateHCID 259091—
ReactantSodium BicarbonateHCID 516892—
SolventBenzeneHCID 241—
Productethyl 5-bromo-3-chloro-1H-indole-2-carboxylateHCID 2833054985.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-bromoindole-2-carboxylic acid ethyl ester (4.00 g, 14.9 mmol), sulfurylchloride (1.8 mL, 22.4 mmol) and benzene (125 mL) was stirred at 90° C. for 2.5 h. The mixture was cooled to room temperature, NaHCO3 (aq., sat.) was added and the mixture extracted with EtOAc. The combined extracts were washed with water, brine and dried over Na2SO4. Concentration and recrystallisation (from toluene) gave the sub-title compound (3.87 g 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705023B2
Source datasetuspto-grants-2010_04
ORD IDord-c74f13d42db74672aa0be2dd38094c51
Source noteuspto-grants-2010_04