HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Methanesulfonyloxymethyl)-6-methyl-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-Methyl-2-nitrobenzenemethanol | HCID 561989 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Methanesulfonyloxymethyl)-6-methyl-nitrobenzene | HCID 15766956 | 97.9% |
Reaction Steps
At 10-15° C., 27 g (0.23 mol) of methanesulfonyl chloride dissolved in 20 ml of CH2Cl2 is dripped into a mixture of 34 g (0.2 mol) of 3-methyl-2-nitrobenzyl alcohol and 27 g (0.27 mol) of triethylamine in 100 ml of CH2Cl2. The reaction mixture is stirred for 1 hour at room temperature and is then extracted with water. The organic phase is dried over MgSO4 and evaporated down. There is obtained as residue 48 g of the title compound as a yellow oil, containing about 10% of the corresponding benzyl chloride as impurity. The crude product is used for the next reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06252083B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-10634ab235344e1d8cb90a9a5c93b753 |
| Source note | uspto-grants-2001_06 |