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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53275Generated: October 26, 2026

Potassium Hydroxide → 4,4-Dimethyl-7-[(dimethylamino)thiocarbonyloxy]-1-tetralone

https://huagongshe.com/reaction/53275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant3,4-Dihydro-7-hydroxy-4,4-dimethyl-1(2H)-naphthalenoneHCID 22101865—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4,4-Dimethyl-7-[(dimethylamino)thiocarbonyloxy]-1-tetraloneHCID 53716818—

Reaction Steps

To a solution of 4,4-dimethyl-7-hydroxy-1-tetralone (XIV) (3.07 g, 16.16 mmol) in water (10.77 mL) containing potassium hydroxide (904 mg) cooled below 10° C. was added N,N-dimethylthiocarbamoyl chloride (2.67 g, 21.6 mmol) in tetrahydrofuran (4.30 mL); the reaction temperature kept below 12° C. After 10 minutes, reaction mixture is made basic by the addition of a 10% aqueous KOH solution (5.39 mL). Product is extracted with ethyl acetate (2×50 mL), organic phases concentrated in vacuo and the residue chromatographed on silica gel (eluted with 10% ethyl acetate in hexane) to give 3.74 g (Y: 84%) of title product; 1H-NMR (CDCl3): δ7.68 (d, J=2.6 Hz, 1H), 7.45 (d, J=8.5 Hz, 1H), 7.27 (dd, J=8.5, 2.6 Hz, 1H), 3.46 (s, 3H), 3.34 (s, 3H), 2.73 (t, J=6.8 Hz, 2H), 2.04 (t, J=6.8 Hz, 2H), 1.41 (s, 6H); MS (DCI) m/e: 278 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618839
Source datasetuspto-grants-1997_04
ORD IDord-47473cc55f5644b6b19ec0dd75be0af0
Source noteuspto-grants-1997_04