Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 86587892 | HCID 86587892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69891250 | HCID 69891250 | — |
Reaction Steps
To 10 mmol of chlorosulphonyl isocyanate dissolved in dichloromethane at 0° C. there are added, dropwise at 0° C., 10 mmol of benzyl alcohol dissolved in dichloromethane and then, after stirring for 1 hour 30 minutes at 0° C., 10 mmol of the compound obtained in Step B of Example 3, dissolved in a mixture of dichloromethane and triethylamine 96/4. After returning to ambient temperature, the reaction mixture is stirred overnight and then separated. The organic phase is washed, dried and evaporated to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716843B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-7bd66164267645feabef521aee8fdd7a |
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| Source note | uspto-grants-2004_04 |
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