HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobutyryl chloride → HCID 19909509, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobutyryl chloride | HCID 70225 | — |
| Reactant | 3-(1-Hydroxytridecyl)-5-trimethylsilylfuran | HCID 15663268 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19909509 | HCID 19909509 | — |
Reaction Steps
tert-Butyl lithium (a 1.7 M solution in pentane; 0.25 ml, 0.43 mmol) was added dropwise to a solution of 4-(1-hydroxytridecyl)-2-trimethylsilylfuran (120.4 mg, 0.36 mmol) in tetrahydrofuran (6 ml) at 0° under argon. After 20 minutes, a solution of 4-bromobutyryl chloride (66 mg, 0.43 mmol) in tetrahydrofuran (1 ml) was added. Stirring was continued at room temperature for 16 hours and the mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was purified by preparative TLC (20×20 cm, 500μ silica plate; developed with 10% ethyl ether/hexane). The title ester was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089485 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-03f2e2504afe49889ff248c57108eea3 |
| Source note | uspto-grants-1992_02 |