HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283123Generated: November 2, 2026
Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate) → HCID 13066475, compound
https://huagongshe.com/reaction/1283123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate) | HCID 86977 | — |
| Reactant | HCID 13066473 | HCID 13066473 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium | HCID 5360545 | — |
| Product | HCID 13066475 | HCID 13066475 | 53.6% |
Reaction Steps
3 g of 5H-[1]benzopyrano[ 2,3-b]pyridin-7-yl-acetone is dissolved in a solution of 0.32 g of metallic sodium in 15 ml of absolute isopropyl alcohol by warming to 50°-60°C. The solution is cooled to 40°C, 3.5 g of 2-methoxyethyl p-toluenesulfonate is added, and the mixture is stirred under reflux for 1.5 hours. The reaction mixture is concentrated, chloroform and water are added to the residue, and the mixture is stirred. The chloroform layer is separated, dried over anhydrous magnesium sulfate and concentrated. The oily residue is column chromatographed over silica gel (100 g) with a mixture of chloroform and ethyl acetate (10:1) as eluent to give 2.0 g of 3-(5H-[1]benzopyrano[ 2,3-b]pyridin-7-yl)-5-methoxy-2-pentanone as a pale yellow transparent oil. nD28 = 1.5764
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974168 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-e3d8e7db89e24e9ab4600ae52246cd7a |
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| Source note | uspto-grants-1976_08 |
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