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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | 3,4-Dihydro-7-hydroxy-4,4-dimethyl-1(2H)-naphthalenone | HCID 22101865 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Dimethyl-7-[(dimethylamino)thiocarbonyloxy]-1-tetralone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618839 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-47473cc55f5644b6b19ec0dd75be0af0 |
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| Source note | uspto-grants-1997_04 |
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