Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178478587HCID 178478587—
SolventDichloromethaneHCID 6344—
ProductHCID 178527410HCID 17852741041.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722683B2
Source datasetuspto-grants-2014_05
ORD IDord-f35ee7329217410e8ebdb54e8f603653
Source noteuspto-grants-2014_05