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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992488Generated: November 3, 2026

(Diethylamino)sulfur trifluoride → HCID 18412755, compound

https://huagongshe.com/reaction/992488

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 18412756HCID 18412756—
SolventDichloromethaneHCID 6344—
ProductHCID 18412755HCID 1841275577.2%

Reaction Steps

To a suspension of (±)-3-[5-chloro-2-[4-(trifluoromethyl)phenyl-methoxy]phenyl]-1,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indole-2-one (Preparation 6, 45 mg, 0.09 mmol) in CH2Cl2 (3 mL), was added dropwise neat diethylaminosulfur trifluoride (0.018 mL, 0.135 mmol) at −78° C. The reaction mixture was warmed to room temperature for 15 minutes and then quenched with water. The organic layer was separated, washed with water, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo to provide the title compound (35 mg, 77% yield). MS m/e 502 (MH−). 1H NMR (CDCl3): δ7.84 (d, J=1.95 Hz, 1H), 7.68 (s, 1H), 7.53 (d, J=8.1 Hz, 2H), 7.36 (dd, J=8.7 Hz, 2.5 Hz, 1H), 7.29 (m, 1H), 7.21 (m, 1H), 7.05 (d, J=8.1 Hz, 2H), 6.81(dd, J=8.8 Hz, 1.1 Hz, 1H), 6.73 (s, 1H), 4,88 (d, 11.0 Hz, 1H), 4.73 (d, J=11.0 Hz,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469042B1
Source datasetuspto-grants-2002_10
ORD IDord-875a74825cf948049d2c910f2a030822
Source noteuspto-grants-2002_10