Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 53810750 | HCID 53810750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18923530 | HCID 18923530 | 94.2% |
Reaction Steps
To a mixture of 2,6-dichloro-3-isopropoxybenzyl alcohol (1.65 g) and triethylamine (808 mg) in dichloromethane was added methanesulfonyl chloride (884 mg) in a few minutes at 5° C. After stirring for half an hour at 5° C., the mixture was washed with diluted hydrochloric acid and then with aqueous sodium bicarbonate solution, dried, and concentrated in vacuo. The residue was crystallized from n-hexane to give 2,6-dichloro-3-isopropoxybenzyl methanesulfonate (2.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574042 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-50d974f3c87f43489a7bce6782018b21 |
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| Source note | uspto-grants-1996_11 |
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