HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182296Erstellt: 26. Oktober 2026
(+)-Pantolactone → (S)-3,3-Dimethylbutane-1,2,4-triol
https://huagongshe.com/reaction/1182296
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (+)-Pantolactone | HCID 736053 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (S)-3,3-Dimethylbutane-1,2,4-triol | HCID 11020933 | 99,9% |
Reaktionsschritte
To a 0° C. solution of 5.01 g (38.5 mmol) of (S)-(+)-pantolactone in 150 mL of methanol was added 3.72 g (98.5 mmol) of sodium borohydride carefully. After gas evolution had subsided, the ice-bath was removed and the reaction mixture was closely monitored, cooling again to 0° C. with an ice-water bath as needed when gas evolution became vigorous. The ice-water bath was removed and the reaction mixture was stirred at room temperature for 4 h. Dowex 50Wx4-400 (H+) resin was added to the solution until the reaction mixture was neutral. The resin was filtered off and the filtrate was concentrated under reduced pressure. The oil was diluted and concentrated with portions of methanol and then toluene. The remaining clear oil was dried under high vacuum to afford 5.16 g (>99%) of (2S)-3,3-dimethyl-1,2,4-butanetriol. 1H-NMR (300 MHz, CDCl3): δ 3.82–3.49 (m, 5H), 3.11 (d, J=4 Hz, 1H), 2.62 (m, 1H), 2.42 (m, 1H), 0.98 (d, J=6 Hz, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07288541B2 |
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| Quelldatensatz | uspto-grants-2007_10 |
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| ORD ID | ord-6b92827c9cd94eac8704af04178f4c8e |
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| Quellennotiz | uspto-grants-2007_10 |
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