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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 1-bromocyclohexanecarboxylate | HCID 3518593 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylate | HCID 22235978 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012075B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-84ab38f8a04f4529a461ba679cfb7d3b |
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| Source note | uspto-grants-2006_03 |
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