4-(5-Ethyl-3,3-dimethyl-2,4-dioxopyrrolidin-1-yl)-2-(trifluoromethyl)benzonitrile → Rac-4-[(4r,5r)-5-ethyl-4-hydroxy-3,3-dimethyl-2-oxopyrrolidin-1-yl]-2-(trifluoromethyl)benzonitrile

HRID 1967339Notes

Reaction equation

HRID 1967339 reaction equation
[CH2:1]([CH:3]1[N:7]([C:8]2[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[C:10]([C:16]([F:19])([F:18])[F:17])[CH:9]=2)[C:6](=[O:20])[C:5]([CH3:22])([CH3:21])[C:4]1=[O:23])[CH3:2].C([BH-](C(CC)C)C(CC)C)(CC)C.[Li+].C1COCC1>>[CH2:1]([C@H:3]1[N:7]([C:8]2[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[C:10]([C:16]([F:17])([F:18])[F:19])[CH:9]=2)[C:6](=[O:20])[C:5]([CH3:22])([CH3:21])[C@H:4]1[OH:23])[CH3:2]

Participants

3

Procedure

Using 4-(5-ethyl-3,3-dimethyl-2,4-dioxopyrrolidin-1-yl)-2-(trifluoromethyl)benzonitrile (120 mg) and lithium tri(sec-butyl)borohydride-THF solution (0.555 mL, 1 mol/L), and in the same manner as in Example 5, the title compound was obtained as a colorless solid (yield: 76 mg, 63%).

Sources & evidence

ORD record
ord-8e0014feb66e42ea96cc80f4a2251da9
Source dataset
uspto-grants-2013_04
Patent number
US08420694B2

Reaction notes

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