HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109391Generated: November 2, 2026
p-Toluenesulfonic acid → HCID 15107107, compound
https://huagongshe.com/reaction/1109391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 15107105 | HCID 15107105 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15107107 | HCID 15107107 | — |
Reaction Steps
983 mg of (3RS,4S)-4-(benzyloxycarbonyl)amino-5-cyclohexylpentene-3-ol was dissolved in 5 ml of dichloromethane, and 4 ml of 2,2-dimethoxypropane and 30 mg of dry p-toluenesulfonic acid were added thereto. The mixture was stirred at room temperature overnight. Then, 100 ml of ethyl acetate was added to the reaction mixture. The mixture was washed with a saturated sodium hydrogencarbonate aqueous solution and with a saturated sodium chloride aqueous solution. Then, the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by-silica gel column chromatography (n-hexane/ethyl acetate=20/1) to obtain 967 mg of (4S,5RS)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-ethenyl-2,2-dimethyloxazolidine as colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05319082 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-318e5504a346410b83e5e1001c9bae07 |
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| Source note | uspto-grants-1994_06 |
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