HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(4-Bromobutyl)-4-thiazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Thiazolidinone | HCID 637591 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Bromobutyl)-4-thiazolidinone | HCID 10847505 | — |
Reaction Steps
A mixture of 4-oxothiazolidine (25 g,) dimethylformamide (500 ml), and KOH (27.16 g) was stirred under N2 at room temperature for 1.5 hours. To the resulting mixture was added 1,4-dibromobutane (101 ml) and stirring was continued at room temperature for 44 hours. The reaction mixture was poured into H2O (1000 ml) and the aqueous mixture was extracted three times with 300 ml portions of ethyl acetate. The combined extracts were washed with H2O (300 ml) and brine (300 ml), dried over Na2SO4, and concentrated in vacuo to an oil. HPLC of a 44.95 g aliquot yielded 7.15 g of an oil which upon distillation yielded a clear liquid, b.p. 134°-137° C/0.12 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041445 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-f5fbe84acd0d425890172681cdda472c |
| Source note | uspto-grants-1991_08 |