HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436854Generated: October 26, 2026
Dichloromethane → 2-Methyl-3-nitrobenzyl methanesulfonate
https://huagongshe.com/reaction/1436854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Methyl-3-nitrobenzyl alcohol | HCID 90289 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-3-nitrobenzyl methanesulfonate | HCID 19369758 | — |
Reaction Steps
200 g 2-Methyl-3-nitro benzylalcohol is added to dichloromethane (2000 ml) and triethylamine (250 ml). Mesyl chloride is added drop wise while maintaining temperature between 0-10° C. and stirred until the completion of reaction. It is further stirred 2 hours at room temperature. Water is added to the reaction mixture and stirred for 10 minutes. Organic layer was separated and washed with brine. Dichloromethane was evaporated to yield the oily brown 2-Methyl-3-nitrobenzyl methanesulfonate (207-210 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07619095B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-1ad5c504a8ef4d32867a9aa8a945ff6c |
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| Source note | uspto-grants-2009_11 |
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