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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744082Generated: October 27, 2026

2-Bromobenzenethiol → Methyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylate

https://huagongshe.com/reaction/1744082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzenethiolHCID 80598—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 1-bromocyclohexanecarboxylateHCID 3518593—
SolventMethanolHCID 887—
ProductMethyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylateHCID 22235978—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 715 mg (3.2 mmol) of methyl 1-bromocyclohexane-1-carboxylate (J. Med. Chem. 1970, 13, 317) in MeOH (5 mL) was added diisopropylethylamine (0.9 mL, 5.2 mmol) and 2-bromobenzenethiol (0.55 mL, 4.7 mmol). The solution was heated to 65° C. under nitrogen for 2 h, then cooled and partitioned between ethyl acetate and 1 M HCl. The organic phase was washed twice with 1 M NaOH and brine, then dried over MgSO4 and concentrated. Purification by flash chromatography (10% EtOAc/hexanes) gave methyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-84ab38f8a04f4529a461ba679cfb7d3b
Source noteuspto-grants-2006_03