Methyl acetoacetate → 5-Methyl-1-phenylhexan-1-one

HRID 357828Notes

Reaction equation

HRID 357828 reaction equation
[C:1](OC)(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[H-].[Na+].C([Li])CCC.[C:16]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)(=[O:23])[CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21].[Al+3].[Cl-].[Cl-].[Cl-]>CCCCCC.C1C=CC=CC=1.O1CCCC1>[OH:4][C:3]1[CH2:5][C:16]([CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])([C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[O:23][C:1](=[O:6])[CH:2]=1.[C:16]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)(=[O:23])[CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21]

Participants

10

Procedure

The title compound was prepared as described in General Method 1 using 14.2 mmol of methyl acetoacetate, 15.6 mmol of NaH 60% dispersion in oil, 14.9 mmol of 1.6M n-butyl lithium in hexane, 14.2 mmol of isoheptanophenone and 50 mL of tetrahydrofuran. Isoheptanophenone was prepared by reacting the appropriate acid chloride with AlCl3 in benzene as described by Vogel in Practical Organic Chemistry 1978, 770-775. Upon concentrating the reaction, a solid precipitated out which was recrystallized from ethyl acetate (m.p. 124°-125° C.). 1H NMR (CDCl3) δ 0.80 (d,d, 6 H), 1.1-1.2 (m, 2 H), 1.15-1.40 (m, 2 H), 1.4-1.5 (m, 1 H), 1.9-2.0 (m, 2 H), 2.88 (d, 1 H), 2.9 (d, 1 H), 3.2 (d, 1 H), 3.3 (d, 1 H), 7.2-7.5 (m, 5 H).

Workup

  1. concentrationUpon concentrating
  2. customthe reaction
  3. customa solid precipitated out which
  4. customwas recrystallized from ethyl acetate (m.p. 124°-125° C.)

Sources & evidence

ORD record
ord-2463a4b90ae54c659724009081d58b07
Source dataset
uspto-grants-1998_11
Patent number
US05840751

Reaction notes

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