HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyl mercaptan → HCID 22103576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyl mercaptan | HCID 10558 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10984709 | HCID 10984709 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22103576 | HCID 22103576 | — |
Reaction Steps
To a solution of 5 equiv. of 2-methyl-1-propanethiol (125 mg, 1.39 mmol) in 1 ml of dry DMF was added 2.5 equiv. of 60% sodium hydride under an argon atmosphere at room temperature. The reaction mixture was stirred for 0.5 hrs. and then a solution of the title compound of Step (B) (160 mg, 0.278 mmol) in 1 ml of DMF was added. The reaction was stirred for 1 hr, diluted with 15 ml of water and extracted with ethyl acetate (3×20 ml). The ethyl acetate extract was washed with 5% lithium chloride (2×30 ml), brine and dried over sodium sulfate. The crude material was purified on a Merck silica column eluting with 40% ethyl acetate/hexane yielding 118 mg (68%) of the title compound of this step as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05846990 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-c979a56315c545638a5ef9155e9eacb9 |
| Source note | uspto-grants-1998_12 |