HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,6-Dichloro-1-methylsulfonyloxymethyl-3-(methoxymethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2,6-Dichloro-3-(methoxymethoxy)benzyl alcohol | HCID 53640739 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dichloro-1-methylsulfonyloxymethyl-3-(methoxymethoxy)benzene | HCID 19603230 | — |
Reaction Steps
To a solution of 2,6-dichloro-3-(methoxymethoxy)benzyl alcohol (1.1 g) and triethylamine (563 mg) in dichloromethane was added a solution of methanesulfonyl chloride (585 mg) in dichloromethane at <20° C. over 5 minutes under nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes and under ice-cooling for 30 minutes. The reaction mixture was washed with saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and evaporated in vacuo to give 1,3-dichloro-2-methanesulfonyloxymethyl-4-(methoxymethoxy)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994368 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-136e26488a2d4c9cbb0a13c1f20ad7fb |
| Source note | uspto-grants-1999_11 |