HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023268Generated: November 4, 2026
2,2,2-Trifluoroethanesulfonyl chloride → HCID 178527410, compound
https://huagongshe.com/reaction/1023268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanesulfonyl chloride | HCID 74242 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178478587 | HCID 178478587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178527410 | HCID 178527410 | 41.1% |
Reaction Steps
To a stirred mixture of N-trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperazin-1-yl)-ethyl]-cyclohexylamine hydrochloride (Intermediate A) (30 mg, 81.5 μmol, Eq: 1.00) in dichloromethane (500 μl) was added at room temperature N,N-diisopropylethylamine (31.6 mg, 42.7 μl, 245 μmol, Eq: 3) and 2,2,2-trifluoroethanesulfonyl chloride (22.3 mg mg, 122 μmol). The mixture was allowed to stir at room temperature over night. The crude reaction diluted with 5 mL sat NaHCO3 and extracted with DCM (2×10 mL). The organic layers were dried over MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 10 g, 0% to 10% MeOH in DCM) to yield the title compound as an white solid (16 mg, 41.1%), MS (ISP) m/z=478.1 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722683B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-f35ee7329217410e8ebdb54e8f603653 |
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| Source note | uspto-grants-2014_05 |
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