HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 465755Erstellt: 25. Oktober 2026
Borohydride → 2-Benzoyloxy-4-hydroxymethylcyclobutanol
https://huagongshe.com/reaction/465755
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Borohydride | HCID 28123 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 2-Benzoyloxy-4-hydroxymethylcyclobutanone | HCID 19794318 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2-Benzoyloxy-4-hydroxymethylcyclobutanol | HCID 19794289 | 101,8% |
Reaktionsschritte
Glacial acetic acid (25 mL) in a 250 mL 3-neck flask was cooled in an ice bath under a stream of nitrogen. Sodium borohydride was added cautiously in portions over a 5 minute period. The ice bath removed and the reagent was used after stirring for 15 minutes at ambient temperature. 2-Benzoyloxy-4-hydroxymethylcyclobutanone (1.43 g, 6.5 mmol) from Step H was dissolved in 45 mL of glacial actetic acid and immediately treated with the above borohydride reagent. After stirring the reaction mixture for 35 minutes, the reaction was quenched with ~2 mL of methanol and the reaction mixture was concentrated in vacuo to a syrup. The syrup was dissolved in 250 mL of ethyl acetate and the ethyl acetate solution was washed with water and 5% aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to give 1.47 g of the title compound which was taken on to the next step without purification; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05153352 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-ff352713a78f4e88bc23c704627f089a |
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| Quellennotiz | uspto-grants-1992_10 |
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