HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 18675620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | benzyl N-(2-hydroxyethyl)carbamate | HCID 280458 | — |
| Reactant | Methyl 3,3-diphenyloxirane-2-carboxylate | HCID 10587027 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18675620 | HCID 18675620 | — |
Reaction Steps
9.8 g (50 mmol) of benzyl (2-hydroxyethyl)carbamate and 12.7 g (50 mmol) of methyl 2,3-epoxy-3,3-diphenylpropionate were dissolved in 80 ml of methylene chloride and, with ice-cooling, 0.95 g (5 mmol) of p-toluenesulfonic acid was added. The reaction mixture was stirred at room temperature for 24 hours and then diluted with methylene chloride and extracted with 2M aqueous sodium hydroxide solution, the organic phase was separated off and dried over sodium sulfate and the solvent was distilled off. The residue (22.2 g of an oil) was directly reacted further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509341B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-a125b0b1550b4cf8b0727e5c35acea60 |
| Source note | uspto-grants-2003_01 |