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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32073Generated: October 25, 2026

4-Methylmorpholine → 5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/32073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonateHCID 11098384—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoro-methanesulfonic anhydride (14.35 mL, 77.3 mmol) was added to a CH2Cl2 (150 mL) solution of 6-hydroxy-3,4-dihydro-2H-naphthalen-1-one (11.40 g, 70.3 mmol), N-methylmorpholine (8.5 mL, 77.3 mmol) and DMAP (130 mg, 1 mmol) in 5 min at −80° C. The mixture was warmed to 0° C. in 1 h then poured into a cold solution of saturated NH4Cl. The mixture was diluted with CH2Cl2 (400 mL), washed with H2O, dried over MgSO4, filtered, and concentrated in vacuo to provide the crude compound which was purified by column chromatography (silica, 0 to 60% CH2Cl2 in hexane) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425631B2
Source datasetuspto-grants-2008_09
ORD IDord-3b582824b37743d5aefae7d5d204232e
Source noteuspto-grants-2008_09