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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667582Generated: October 29, 2026

Triethylamine → Methyl 2-(cyclobutylsulfanyl)benzoate

https://huagongshe.com/reaction/1667582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBromocyclobutaneHCID 78110—
ReactantMethylthiosalicylateHCID 6932478—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(cyclobutylsulfanyl)benzoateHCID 57448173113.6%

Reaction Steps

To methylthiosalicylate (3.92 mL, 28.5 mmol) in DMF at 0° C. was added triethylamine (3.97 mL, 28.5 mmol) then cyclobutyl bromide (5.00 g, 37.0 mmol). The ice bath was removed and the reaction was stirred at rt for 1 h then heated to 50° C. overnight. After cooling to rt, diethyl ether was added and the mixture was filtered. The filtrate was diluted with ethyl acetate, then washed with water (6×) and brine (1×). The organic layer was dried (MgSO4), filtered and concentrated to provide a yellow oil. The yellow oil was dissolved in CH2Cl2 (143 mL) and MCPBA (˜75%, 19.7 g, ca. 85.5 mmol) was added. The reaction was stirred for 2.5 h, then was cooled to 0° C. 1 N NaOH was added, and the reaction was stirred for 5 min. The layers were separated, and the organic layer was washed with 1 N NaOH (2×). The aqueous layer was back-extracted with CH2Cl2. The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated to provide 2A as a clear oil (7.20 g). LC-MS: 255.01 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044242B2
Source datasetuspto-grants-2011_10
ORD IDord-912ae614ecf74899a66370d57a519b3f
Source noteuspto-grants-2011_10