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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040459Generated: October 30, 2026

Triethylamine → HCID 59676053, compound

https://huagongshe.com/reaction/2040459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67239678HCID 67239678—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59676053HCID 59676053—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 8-methyl-6,11-dihydro-5-thia-11-aza-benzo[a]fluoren-8-ol (180 mg, 0.711 mmol) in CH2Cl2 (20 mL), Et3N (129 μL, 0.924 mmol) was added dropwise followed by CF3(CF2)3SO2F (153 μL, 0.853 mmol) at 0° C. The reaction mixture was slowly warmed up to 25° C. over 2 hours. Then CH2Cl2, water, and saturated aqueous NaHCO3 solution were added to the mixture. The aqueous layer was extracted with CH2Cl2 and the organic layers were washed with brine, dried, and concentrated. Flash chromatography purification (12% EtOAc/Hexane) was used to yield the title as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580840B2
Source datasetuspto-grants-2013_11
ORD IDord-38014307c9274b44a382d4e5074328f8
Source noteuspto-grants-2013_11