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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158832Generated: November 1, 2026

2-Bromobenzenethiol → HCID 66842178, compound

https://huagongshe.com/reaction/1158832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzenethiolHCID 80598—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66841803HCID 66841803—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 66842178HCID 6684217880.7%

Reaction Steps

—Sulfuryl chloride (1.08 ml, 13.4 mmol) was added to a solution of 2-bromobenzenethiol (1.27 g, 6.69 mmol) in dichloromethane (45 ml). The reaction mixture was stirred at room temperature for 15 min. and concentrated under reduced pressure. The resulting material was dissolved in diethyl ether and added dropwise to a solution of [1-(3,5-difluoro-benzyl)-1H-indol-6-yl]-methyl-carbamic acid tert-butyl ester (Example 6, method 1, step i; 2.50 g, 6.71 mmol) in diethyl ether (45 ml). The reaction mixture was stirred for 3.5 h and then poured into a saturated aqueous solution of sodium hydrogencarbonate. The product was extracted into ethyl acetate; the combined organic phases were washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Column chromatography (heptane/ethyl acetate 9:1→8:2) afforded [3-(2-bromo-phenylsulfanyl)-1-(3,5-difluoro-benzyl)-1H-indol-6-yl]-methyl-carbamic acid tert-butyl ester (3.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812036B2
Source datasetuspto-grants-2010_10
ORD IDord-fd7626e37cd24b5da0ddea0673e71d5c
Source noteuspto-grants-2010_10