HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4,8-Dichloro-5-methyl-6-ethoxycarbonylthiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 8-Chloro-6-ethoxycarbonyl-5-methylthiochroman-4-ol | HCID 23450667 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,8-Dichloro-5-methyl-6-ethoxycarbonylthiochroman | HCID 22118389 | 116.1% |
Reaction Steps
1.0 Gram (3.5 mmol) of 4-hydroxy-5-methyl-6-ethoxycarbonyl-8-chlorothiochroman was dissolved in 5 ml of methylene chloride, and 0.72 ml (5.2 mmol) of triethylamine and 0.4 ml (5.2 mmol) of methanesulfonyl chloride were added with an ice bath cooling. The mixture was stirred at room temperature for 1 hour. After the completion of the reaction, an organic layer was washed with 2N hydrochloric acid and with a saturated sodium hydrogencarbonate aqueous solution and dried over anhydrous sodium sulfate, and the solvent was distilled off to give 1.24 g (yield 100%) of 4,8-dichloro-5-methyl-6-ethoxycarbonylthiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159904 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-f78baf194a5f43f8a5b957b850dcd66e |
| Source note | uspto-grants-2000_12 |