HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Benzyl (2R)-2-Benzyl-5-tert-butylmercapto-4-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Benzyl (2R)-2-Benzyl-3-chloromethylcarbonylpropionate | HCID 10449338 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl (2R)-2-Benzyl-5-tert-butylmercapto-4-oxopentanoate | HCID 15018115 | 73% |
Reaction Steps
To tert-butylmercaptan (0.11 ml) in dimethylformamide (5 ml) at 0° C. was added potassium bis(trimethylsilyl)amide in toluene (1.80 ml, 0.90 mmol, 0.5M) followed by the resultant compound from Example 34 (259.6 mg, 0.785 mmol) in dimethylformamide (3 ml). After 16 h at room temperature the mixture was diluted with ethyl acetate, washed with water and brine, then dried over Na2SO4 and evaporated. Chromatography of the residue on silica gel with 10% ethyl acetate in hexane afforded 219.6 mg (73%) of a colorless oil. 1H NMR (CDCl3) δ7.10-7.40 (m,10H), 5.07 (s,2H), 3.25 (s,2H), 3.18-3.29 (m,1H), 2.97-3.07 (m,2H), 2.78 (dd,1H), 2.71 (dd,1H), 1.25 (s,9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05063208 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-3b137e8635dc419084ff4b5fb4c72d5d |
| Source note | uspto-grants-1991_11 |