HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 69224758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzenemethanethiol, alpha,alpha-diphenyl- | HCID 77281 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69224758 | HCID 69224758 | — |
Reaction Steps
To a suspension of sodium hydride (989 mg, 24.47 mmol) in anhydrous DMF (60 mL) was added portion wise triphenylmethanethiol. After 15 minutes of stirring, ethyl 5-bromovalerate (2.8 mL, 17.48 mmol) was injected and the mixture was stirred at ambient conditions for 24 h. The reaction mixture was portioned between ether and saturated ammonium chloride. The water phase was extracted several times with ether. The recombined organic layer was washed with brine, dried, filtered and evaporated. The crude was flashed using 5-10% ethyl acetate in hexanes. 1H-NMR(CDCl3, 400 MHz: 1.23(t, J=7.0 Hz, 3H); 1.42(m, 2H); 1.59(m, 2H); 2.16(m, 4H); 4.09(q, J=7.0 Hz, 2H), 7.21-7.30, 7.42(m, 15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365091B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-116ca048a2ba46f5b0c5a43a63fdb997 |
| Source note | uspto-grants-2008_04 |