HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-(2,3-Dihydrobenzo[b][1,4]dioxin-2-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-2-(Hydroxymethyl)-1,4-benzodioxane | HCID 6541029 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (S)-(2,3-Dihydrobenzo[b][1,4]dioxin-2-yl)methyl methanesulfonate | HCID 11128529 | — |
Reaction Steps
To a solution of 0.410 g (2.467 mM) of (R)-2-hydroxymethyl-1,4-benzodioxane and 0.52 ml (3.70 mM) of triethylamine in 30 ml of diethyl ether was added 0.21 ml (2.71 mM) of methanesulfonyl chloride dropwise with ice-cooling and the mixture was stirred for 0.5 hour. This reaction mixture was poured in aqueous solution of sodium hydrogen carbonate and extracted with 2 portions of ethyl acetate. The organic layers were combined and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was passed through a short silica gel column (hexane-ethyl acetate=3/1 to 2/1) to provide crude (S)-2-methanesulfonyloxymethyl-1,4-benzodioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235731B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-749ad15eb049458480c433e1f282c4b9 |
| Source note | uspto-grants-2001_05 |