Lithium borohydride → HCID 10715906, compound

HRID 2229901Notes

Reaction equation

HRID 2229901 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH:12]=[CH:11][C:10]([C:13]2[CH:18]=[CH:17][C:16]([I:19])=[CH:15][CH:14]=2)=[C:9]1[CH:20]=[O:21])=[O:7])([CH3:4])([CH3:3])[CH3:2].[Li+].[BH4-]>C1COCC1>[C:1]([O:5][C:6]([N:8]1[CH:12]=[CH:11][C:10]([C:13]2[CH:14]=[CH:15][C:16]([I:19])=[CH:17][CH:18]=2)=[C:9]1[CH2:20][OH:21])=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

4

Procedure

A solution of 6(400 mg, 1.0 mmol) in anhydrous THF (12 mL) under argon was cooled to −20 to −25° C. and LiBH4 (55 mg, 2.5 mmol) was added in portions. The reaction was monitored by TLC (silica, hexanes/ethyl acetate (4:1)), and when no starting material was detected (20-25 min), the reaction was quenched with cold water (30 mL). The aqueous layer was extracted with CH2Cl2 and the organic layer was dried (Na2SO4), concentrated, and purified by flash column chromatography [silica, hexanes/ethyl acetate containing 1% Et3N (3:1)] yielding a gum (330 mg, 82%). 1H NMR δ 1.62 (s, 9H), 3.61 (br, 1H), 4.66 (d, J=7.2 Hz, 2H), 6.25 (d, J=3.6 Hz, 1H), 7.18 (d, J=8.1 Hz, 2H), 7.22 (d, J=3.6 Hz, 1H), 7.71 (d, J=8.1 Hz, 2H); 13C NMR δ 27.8, 55.3, 84.7, 92.4, 111.2, 121.3, 127.9, 130.0, 130.4, 134.1, 137.5, 149.8; FAB-MS obsd 399.0336, calcd 399.0331 (C16H18INO3).

Workup

  1. custom(20-25 min)
  2. customthe reaction was quenched with cold water (30 mL)
  3. extractionThe aqueous layer was extracted with CH2Cl2
  4. dry with materialthe organic layer was dried (Na2SO4)
  5. concentrationconcentrated
  6. custompurified by flash column chromatography [silica, hexanes/ethyl acetate containing 1% Et3N (3:1)]

Sources & evidence

ORD record
ord-a950da302b2d408aada2e8ccb5626cb4
Source dataset
uspto-grants-2002_07
Patent number
US06420648B1

Reaction notes

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