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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370641Generated: October 30, 2026

2,2,2-Trifluoroethyl trichloromethanesulphonate → HCID 68195093, compound

https://huagongshe.com/reaction/2370641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethyl trichloromethanesulphonateHCID 90027—
ReactantSodium BicarbonateHCID 516892—
Reactant4,4-Dimethyl-7-nitro-1,2,3,4-tetrahydroisoquinolineHCID 21959655—
SolventDimethylformamideHCID 6228—
ProductHCID 68195093HCID 68195093—

Reaction Conditions

Temperature60 °C

Reaction Steps

2,2,2-Trifluoroethyl trichloromethanesulfonate (1.8 g, 6.40 mmol) was added to a solution of 4,4-dimethyl-7-nitro-1,2,3,4-tetrahydroisoquinoline (0.8 g, 3.88 mmol) and sodium bicarbonate (0.66 g, 7.86 mmol) in N,N-dimethylformamide (50 mL). The reaction mixture was stirred at 60° C. for 16 hour. The mixture was concentrated, and CH2Cl2 (70 mL) and water (70 mL) were added to the residue. After separation, the aqueous layer was extracted with CH2Cl2 again. The combined organic layers were washed with saturated aqueous NaCl (1×150 mL), dried over Na2SO4, filtered, and concentrated to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710065B2
Source datasetuspto-grants-2014_04
ORD IDord-b7b2fb5d72794d55a8a79d5ab467f5f5
Source noteuspto-grants-2014_04