Dibenzofuran → Ethyl 3-hydroxy-3-(2-phenylethyl)hexanoate

HRID 1823648Notes

Reaction equation

HRID 1823648 reaction equation
[Mg].C1C2C3C=CC=CC=3OC=2C=CC=1.C(Br)C=C.C[Si](C)(Cl)Cl.[C:24]1([CH2:30][CH2:31][C:32](=[O:36])[CH2:33][CH2:34][CH3:35])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.Cl[CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40]>C1COCC1>[OH:36][C:32]([CH2:31][CH2:30][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)([CH2:33][CH2:34][CH3:35])[CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40]

Participants

8

Procedure

Magnesium (9.1 g, 0.374 mole) was suspended in THF (99 mL) containing dibenzofuran (1.4109 g) as an internal standard substance and allyl bromide (0.28 g) was added at 31° C. in a thin stream. Thereto was added 2.5 mL of a mixed solution (143 mL) of dimethyldichlorosilane (1.84 g, 14.2 mmole), 1-phenyl-3-hexanone (47.1 g, 0.267 mole), ethyl chloroacetate (34.8 g, 0.284 mole), allyl bromide (0.28 g, 2.3 mmole) and THF (49 mL) at 30° C. in a thin stream. After 18 min, exothermic heat was observed and the internal temperature rose to 32.5° C. After 34 min from the addition in a thin stream, the remaining mixed solution was added at an internal temperature of 32-36° C. over 3 hr in a thin stream. Thereafter, ethyl chloroacetate (10.2 g, 83.2 mmole) was added at an internal temperature of 32-35° C. over 1 hr in a thin stream and thermally insulated at an internal temperature of 36° C. for 1 hr. The title compound in the reaction mixture was analyzed and a reaction mixture containing the title compound (52.5 g, yield 74.3%) was obtained (quantitative analysis by HPLC). The NMR data were the same as in Example 1.

Workup

  1. additionwas added at 31° C. in a thin stream
  2. temperatureexothermic heat
  3. customrose to 32.5° C
  4. additionAfter 34 min from the addition in a thin stream
  5. additionthe remaining mixed solution
  6. additionwas added at an internal temperature of 32-36° C. over 3 hr in a thin stream
  7. waitthermally insulated at an internal temperature of 36° C. for 1 hr

Sources & evidence

ORD record
ord-d915062d46984bb3b9dddf3548c17750
Source dataset
uspto-grants-2006_05
Patent number
US07038075B2

Reaction notes

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