HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl 2-(cyclopropylmethyl)-1,3-dithiane-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | Ethyl 1,3-dithiane-2-carboxylate | HCID 88552 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(cyclopropylmethyl)-1,3-dithiane-2-carboxylate | HCID 22285400 | — |
Reaction Steps
To a flamed dried flask is added dry toluene (80 mL) and sodium hydride (60%, 33.5 mmol, 1.34 g). The reaction is cooled in a ice bath and a solution of ethyl 1,3 dithiane carboxylate (52 mmol, 10 g) and bromomethyl cyclopropane (62.4 mmol, 8.42 g) in DMF (24 mL) are added dropwise over 10 minutes. The ice bath is removed and the reaction is stirred for 18 h. Water is added (50 mL) and the organic layer is separated. The organic layer is washed with brine, dried (Na2SO4), and concentrated to a yellow oil (12 g, 92%). LC-ES/MS: 247.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153624B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-2b7089650b25413781be88d029022323 |
| Source note | uspto-grants-2012_04 |