Aluminium lithium hydride → HCID 86701294, compound

HRID 1627030Notes

Reaction equation

HRID 1627030 reaction equation
[CH3:1][C@@H:2]1[O:6][C:5](=[O:7])[C@H:4]([O:8][CH2:9][C:10]([CH3:12])=[CH2:11])[C@H:3]1[O:13][CH2:14][C:15]([CH3:17])=[CH2:16].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH3:12][C:10](=[CH2:11])[CH2:9][O:8][C@H:4]([C@@H:3]([O:13][CH2:14][C:15]([CH3:17])=[CH2:16])[C@@H:2]([OH:6])[CH3:1])[CH2:5][OH:7]

Participants

4

Procedure

To a solution of (3R,4S,5S)-5-methyl-3,4-bis(2-methylallyloxy)dihydrofuran-2(3H)-one (1 g, 4.16 mmol) in THF (10 mL) at 0° C. was added 1.0 M LAH (9.57 mL, 9.57 mmol) in THF over 15 min. The mixture was warmed to room temperature and stirred for 2 h, then carefully added dropwise to an ice cold saturated aqueous ammonium chloride (NH4Cl) solution (100 mL). The phases were separated and the aqueous layer was extracted with DCM. The combined organic layers were dried over sodium sulfate (Na2SO4), filtered, and the filtrate was concentrated. Purification by flash chromatography (SiO2) afforded the title compound as a colorless oil (920 mg, 90%): 1H NMR (400 MHz, CDCl3) δ 4.99 (d, J=7.8 Hz, 2H), 4.91 (d, J=8.9 Hz, 2H), 4.09-3.92 (m, 5H), 3.93-3.83 (m, 1H), 3.82-3.73 (m, 1H), 3.70 (q, J=4.7 Hz, 1H), 3.39 (dd, J=6.0, 5.0 Hz, 1H), 3.14 (s, 1H), 2.46 (s, 1H), 1.77 (s, 3H), 1.76 (s, 3H), 1.26 (d, J=6.3 Hz, 3H); 13C NMR (101 MHz, CDCl3) δ 141.95, 141.75, 112.99, 112.79, 81.57, 79.41, 75.52, 74.57, 67.60, 61.33, 19.67, 19.63, 19.61.

Workup

  1. customThe phases were separated
  2. extractionthe aqueous layer was extracted with DCM
  3. dry with materialThe combined organic layers were dried over sodium sulfate (Na2SO4)
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated
  6. customPurification by flash chromatography (SiO2)

Sources & evidence

ORD record
ord-fb310a41cd4e4c7cb6eff4b60214fd6a
Source dataset
uspto-grants-2014_07
Patent number
US08785479B2

Reaction notes

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