HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 1,3-Benzothiazol-6-ylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-(Hydroxymethyl)benzothiazole | HCID 17860385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethylene glycol water | HCID 20437942 | — |
| Product | 1,3-Benzothiazol-6-ylmethyl methanesulfonate | HCID 59216292 | — |
Reaction Steps
1,3-benzothiazol-6-ylmethanol (1.56 g, 0.00944 mol) and N,N-diisopropylethylamine (2.47 mL, 0.0142 mol) were stirred in methylene chloride (16 mL). The reaction mixture was cooled in an ethylene glycol/water (4/1)/dry ice bath. To the solution was added dropwise a solution of methanesulfonyl chloride (1.10 mL, 0.0142 mol) in DCM (2 mL). After 30 min the reaction mixture was quenched by adding water, and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give the desired product which was directly used in the next step without purification. LCMC: (M+H)+=244.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683060B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-7206752730114ca78d57f3ef611ce5cb |
| Source note | uspto-grants-2010_03 |