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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853122Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 178477576, compound

https://huagongshe.com/reaction/853122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178477569HCID 178477569—
SolventDichloromethaneHCID 6344—
ProductHCID 178477576HCID 17847757693%

Reaction Steps

A solution of 0.71 g (1.87 mmol) of trans 4-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-cyclohexylamine in 5 mL of CH2Cl2 was treated with 0.64 mL (3.74 mmol) of DIPEA and 0.24 mL (1.87 mmol) of benzenesulfonylchloride and stirred at RT for 3 hrs. Distribution of the crude mixture between a diluted aqueous solution of HCl and Et2O, drying of the combined organic phases over Na2SO4 and chromatography on silica gel with EtOAc/heptane 1:1 gave 0.9 g (93%) of trans-N-[4-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-cyclohexyl]-benzenesulfonamide as a light yellow semisolid, MS: 518 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253282B2
Source datasetuspto-grants-2007_08
ORD IDord-1d5233e58c124aff91d41afb6a9244e1
Source noteuspto-grants-2007_08