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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470491Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → HCID 88921461, compound

https://huagongshe.com/reaction/1470491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68281903HCID 68281903—
SolventDichloromethaneHCID 6344—
ProductHCID 88921461HCID 88921461—

Reaction Steps

To a solution of (4-hydroxy-8-methylnaphthalen-1-yl)(morpholino)methanone (above Step-7 intermediate) (1 equiv) in dry CH2Cl2 (4 mL) under nitrogen was added DIPEA (3 equiv) at 0° C. and the mixture was stirred for 10 min. To this, Tf2O (1.5 equiv) was added drop wise and the reaction mixture was stirred for another 1.5 h at 0° C. Then it was slowly quenched with water (10 mL) and the aqueous layer was extracted with CH2Cl2 (4×10 mL). The combined organic layer was washed with water (10 mL), brine (10 mL), dried (Na2SO4) and filtered. The solvent was removed under reduced pressure and the residue was purified by column to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006442B2
Source datasetuspto-grants-2015_04
ORD IDord-2ad5e0a0726f4bb08585e34925e7fe98
Source noteuspto-grants-2015_04