HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974845Generated: October 29, 2026
Hydrochloric Acid → 8-Chloro-6-ethoxycarbonyl-5-methylthiochroman-4-ol
https://huagongshe.com/reaction/974845
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Methyl-6-ethoxycarbonyl-8-chlorothiochroman-4-one | HCID 10902158 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Chloro-6-ethoxycarbonyl-5-methylthiochroman-4-ol | HCID 23450667 | 97.3% |
Reaction Steps
88.4 g (311 mmol) of the 8-chloro-6-ethoxycarbonyl-5-methylthiochroman-4-one obtained in the above step (5) was dissolved in 200 ml of ethanol, and further dissolved in 200 ml of dichloromethane. This solution was cooled to 5°~10° C., and 5.9 g (155 mmol) of sodium borohydride was added. The reaction mixture was stirred at the above temperature for 30 minutes, and further stirred at room temperature for 3 hours. Then, the reaction mixture was poured into 400 ml of a 5% hydrochloric acid aqueous solution and extracted with 900 ml of dichloromethane, and then the resultant organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off to give 86.8 g (yield 97%) of 8-chloro-6-ethoxycarbonyl-5-methylthiochroman-4-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607898 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-2d0c6b6b12b045d6bda5e58f3e858e4f |
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| Source note | uspto-grants-1997_03 |
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