HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35491Generated: October 29, 2026
2-Dimethylaminopyridine → HCID 56613713, compound
https://huagongshe.com/reaction/35491
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(1-Hydroxy-6-methoxycarbonylhexyl)-4-(3-t-butyldimethylsilyloxy-1-octenyl)-2-cyclopentenone | HCID 57178898 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56613713 | HCID 56613713 | 25% |
Reaction Steps
480 mg (1.0 mmole) of 4-(3-t-butyldimethylsiloxy-1-octenyl)-5-(1-hydroxy-6-methoxycarbonylhexyl)-2-cyclopentenone was dissolved in 5 ml of dichloromethane, followed by addition of 730 mg (6 mmoles) of dimethylaminopyridine and 230 microliters (3.0 mmoles) of methanesulfonyl chloride in this order. The mixture was stirred at 40° C. for 2 hours. An aqueous solution of sodium bicarbonate was added, and the mixture was stirred with dichloromethane. The organic layers were combined, washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The dried product was filtered, concentrated and subjected to silica gel column chromatography (silica gel 20 g; eluent, hexane:ethyl acetate=10:1) to give 114 mg (yield 25%) of 4-(3-t-butyldimethylsilyloxy-1-octenyl)-5-(6-methoxycarbonylhexylidene)-2-cyclopentenone. The resulting compound had the following spectral data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766147 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-fe1403fc89004298bf00072c68230820 |
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| Source note | uspto-grants-1988_08 |
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