5,5-Dimethyl-1,3-dioxane-2-propionaldehyde → 3-(5,5-Dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-ol

HRID 2414797Notes

Reaction equation

[F:1][C:2]1[CH:7]=[CH:6][C:5]([Mg]Br)=[CH:4][CH:3]=1.[CH3:10][C:11]1([CH3:21])[CH2:16][O:15][CH:14]([CH2:17][CH2:18][CH:19]=[O:20])[O:13][CH2:12]1>C1COCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:19]([OH:20])[CH2:18][CH2:17][CH:14]2[O:15][CH2:16][C:11]([CH3:10])([CH3:21])[CH2:12][O:13]2)=[CH:4][CH:3]=1

Participants

Conditions

Temperature: -70 °C

Procedure

4-Fluorophenyl magnesium bromide (8.7 ml, 2M solution in ether, 17.44 mmol) was added to a solution of 5,5-dimethyl-1,3-dioxane-2-propanal (2 g, 11.62 mmol) (Step 2) in THF (50 ml) at −70° C. After stirring at −70° C. for 2 hr, the reaction mixture was warmed to room temperature and stirred overnight. The reaction was quenched with water and extracted with ethyl acetate. The organic fractions were combined and washed successively with water and brine. After drying (MgSO4), filtration and concentration, the crude compound (3.5 g) was chromatographed to give α-(4-fluorophenyl)-5,5-dimethyl-1,3-dioxane-2-propanol (2.73 g) as a white solid: mp (DSC) 84° C. Anal Calc'd. for C15H21FO3: C, 67.14; H, 7.89. Found: C, 67.18; H, 7.98.

Workup

temperaturethe reaction mixture was warmed to room temperature
stirringstirred overnight
customThe reaction was quenched with water
extractionextracted with ethyl acetate
washwashed successively with water and brine
customAfter drying
filtration(MgSO4), filtration and concentration
customthe crude compound (3.5 g) was chromatographed

Sources & evidence

ORD record: ord-ddbc1d924e834ee7925edf1626573a6a
Source dataset: uspto-grants-2004_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06815460B2

Reaction notes

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