HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568730Generated: November 2, 2026
Hydrochloric Acid → HCID 20150393, compound
https://huagongshe.com/reaction/568730
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-(6-Chloro-2-methyl-3,4-dihydro-2H-1-benzopyran-2-yl)ethan-1-ol | HCID 20150419 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20150393 | HCID 20150393 | 81.2% |
Reaction Steps
In a nitrogen atmosphere, 11.0 g (0.0495 mol) of 6-chloro-3,4-dihydro-2-(2-hydroxyethyl)-2-methyl-2H-benzopyran was dissolved in 50 ml of pyridine, the solution was cooled to 0° C. and, with vigorous stirring, 11.3 g of p-toluenesulfonyl chloride was added gradually thereto. After stirring at 0° C. for 1 hour, the reaction mixture was poured into 300 ml of dilute hydrochloric acid and extracted with diethyl ether. The ether layer was washed with water, dried over anhydrous magnesium sulfate and filtered. Low-boiling substances were distilled off from the filtrate under reduced pressure, and the residue was purified by silica gel column chromatography to give 15.3 g of 6-chloro-3,4-dihydro-2-methyl-2-[2-(p-toluenesulfonyloxy)ethyl]-2H-benzopyran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04728650 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-9a94aa35358b4aed983d42ca279a7d6e |
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| Source note | uspto-grants-1988_03 |
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