Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 28414031 | HCID 28414031 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86628048 | HCID 86628048 | 94% |
Reaction Steps
4-[(2-Hydroxyethoxy)methyl]benzonitrile (5.5 g, 30.5 mmol; see step (i) above) was dissolved in DCM (61 mL) and cooled to −10° C. Triethylamine (5 mL, 36.5 mmol) and methanesulfonyl chloride (3.84 g, 33.5 mmol) were added and the resulting mixture was stirred at below −5° C. for 1.5 h and then at RT overnight. Dichloromethane (200 mL) was added and the mixture was washed with water (2×100 mL) and then dried over Na2SO4. Evaporation of solvents gave 7.3 g (94%) of the title compound, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928225B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-0ba14a67b71840baaf38da53dca4e3e8 |
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| Source note | uspto-grants-2011_04 |
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