HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 10802477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54725366 | HCID 54725366 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10802477 | HCID 10802477 | — |
Reaction Steps
To a room temperature solution of methyl 3-hydroxy-5-methoxybenzo[b]thiophene -2-carboxylate (1.00 g, 4.2 mmol) [Connor, et al., J. Med. Chem. 35:959 (1992)]in 20 mL of DMSO is added potassium t-butoxide (494 mg, 4.41 mmol) followed by bromoacetonitrile (878 μL, 12.58 mmol). The mixture is stirred at room temperature for 1.5 hours, then poured into ethyl acetate and 1N HC1. The organic layer is washed with 1N HCl, followed by several portions of brine, and dried over MgSO4. Filtration followed by removal of solvent in vacuo and recrystallization of the residue from ethyl acetate:hexane gives 413 mg. An additional crop of 112 mg can be obtained from the mother liquor, mp 159.5°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612330 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-2b4c18741f974424a9e951a9a68d4554 |
| Source note | uspto-grants-1997_03 |