HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl mercaptan → 864266-67-1
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 864266-67-1 | HCID 28413190 | 91.2% |
Reaction Steps
Add sodium ethoxide (12 mL of 21% w/v in ethanol, 36 mmol) to a solution of 2-methyl-2-propanethiol (4.06 mL, 36 mmol) in anhydrous ethanol (90 mL) at 0° C. under nitrogen atmosphere. Stir the solution and allow it to warm to room temperature over 30 min. Add 6-chloronicotinonitrile (5 g, 36 mmol) and then heat the reaction to reflux overnight. Cool to room temperature, add saturated aqueous NaHCO3 and concentrate in vacuo. Extract into EtOAc or dichloromethane and wash with brine. Dry over MgSO4 and concentrate in vacuo to give the desired intermediate as orange crystals (6.31 g, 91%). MS (ES+) m/z: 193 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022062B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-1cd07deb21fe409bb4588cc3c30b815c |
| Source note | uspto-grants-2011_09 |