HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrofluoric Acid → 3-(5-Hydroxypent-1-yl)cyclopentene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(5-[(1,1-Dimethylethyl)dimethylsiloxy]pent-1-yl)cyclopentene | HCID 13924073 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(5-Hydroxypent-1-yl)cyclopentene | HCID 15053015 | — |
Reaction Steps
3-(5-[(1,1-Dimethylethyl)dimethylsiloxy]pent-1-yl)cyclopentene (300 g, 1.170 moles) is diluted with acetonitrile (3000 ml) and a 40% stock solution of hydrofluoric acid (166 ml) is added. The reaction is stirred at room temperature for 10 minutes and then slowly neutralized with a saturated solution of sodium bicarbonate. The reaction is partitioned between ether (1500 ml) and the aqueous phase extracted with ether (1×1000 ml). The organic layers are combined and the solvent volume is reduced under vacuum. The residue is dried over anhydrous sodium sulfate and the remaining solvent removed leaving a clear, colorless oil. The product is kugelrohred under vacuum leaving a product sufficiently pure for the next reaction (171 g, 1.11 moles).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689345 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-44bfa0d5f31a44aa9684818b80bf5a65 |
| Source note | uspto-grants-1987_08 |