HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667582Generated: October 29, 2026
Triethylamine → Methyl 2-(cyclobutylsulfanyl)benzoate
https://huagongshe.com/reaction/1667582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Bromocyclobutane | HCID 78110 | — |
| Reactant | Methylthiosalicylate | HCID 6932478 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(cyclobutylsulfanyl)benzoate | HCID 57448173 | 113.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044242B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-912ae614ecf74899a66370d57a519b3f |
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| Source note | uspto-grants-2011_10 |
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