(+)-Pantolactone → (S)-3,3-Dimethylbutane-1,2,4-triol

HRID 1182296

반응식

HRID 1182296 반응식
[CH3:1][C:2]1([CH3:9])[C@H:7]([OH:8])[C:5](=[O:6])[O:4][CH2:3]1.[BH4-].[Na+]>CO>[CH3:1][C:2]([CH3:9])([CH2:3][OH:4])[C@H:7]([OH:8])[CH2:5][OH:6]

참가 물질

4

반응 조건

온도
0 °C

실험 절차

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).

후처리

  1. customthe ice-bath was removed
  2. customThe ice-water bath was removed
  3. additionDowex 50Wx4-400 (H+) resin was added to the solution until the reaction mixture
  4. filtrationThe resin was filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. additionThe oil was diluted
  7. concentrationconcentrated with portions of methanol
  8. customThe remaining clear oil was dried under high vacuum

출처 및 근거

ORD 기록
ord-6b92827c9cd94eac8704af04178f4c8e
출처 데이터셋
uspto-grants-2007_10
특허 번호
US07288541B2

연결된 노트

불러오는 중…