Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | HCID 19068273 | HCID 19068273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54028471 | HCID 54028471 | — |
Reaction Steps
600 mg (20 mmol) of sodium hydride (80% in oil) and 50 ml of DMF were introduced into a round-bottomed flask under a stream of nitrogen. The mixture was cooled to 0° C. and a solution of 5.5 g (20 mmol) of 3-(1-adamantyl)-4-methoxyphenol in 100 ml of DMF was added dropwise, tand he mixture was stirred until the evolution of gas had ceased. A solution of 3.3 g (26 mmol) of dimethylthiocarbamoyl chloride in 50 ml of DMF was then added thereto and the mixture was stirred for eight hours at room temperature. The reaction medium was poured into water and extracted with ethyl acetate. The organic phase was separated out after settling had taken place, washed with water, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a column of silica, eluted with a mixture of dichloromethane and hexane (70/30). After evaporation of the solvents, 3.1 g (46%) of the expected compound having a melting point of 162°-4° C., were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786379 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-888a4d2b87394b6ca0878abdbb078863 |
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| Source note | uspto-grants-1998_07 |
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