HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → HCID 178475410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 178475771 | HCID 178475771 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178475410 | HCID 178475410 | 43.1% |
Reaction Steps
To a -78° C. THF (6 mL) solution of compound 13 (trans:cis ratio, 2:1, 600 mg; 1.2 mmol) was added 1N THF solution of sodium bis(trimethylsilyl)amide (1.2 mL, 1.2 mmol), and the resulting solution was stirred for 15 min. Pivaloyl chloride (150 mg, 1.24 mmol) was added, and the solution was stirred for 30 min at -78° C. and for 1.5 h at room temperature. The reaction mixture was partitioned between pH 4.0 aqueous buffer and ether. The organic phase was dried (MgSO4) and concentrated. The residue was purified by silica gel chromatography (1:1/Et2O:hexane) to afford 300 mg (43%) of the title product as a mixture of trans and cis (3:2) isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05175283 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-f168c186810f4dce936ca0972beea46d |
| Source note | uspto-grants-1992_12 |