Ethyl bromoacetate → Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoate

HRID 354573Notes

Reaction equation

HRID 354573 reaction equation
[C:1]([O:4][CH:5]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:6][C:7](=[O:9])[CH3:8])(=[O:3])[CH3:2].BrC[C:22]([O:24][CH2:25][CH3:26])=[O:23].[Cl-].[CH2:28]([Al+]CC)C>C1COCC1.[Zn]>[C:1]([O:4][CH:5]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:6][C:7]([OH:9])([CH3:28])[CH2:8][C:22]([O:24][CH2:25][CH3:26])=[O:23])(=[O:3])[CH3:2]

Participants

6

Procedure

A solution of 6-(2,4-dichlorophenyl)-2-oxo-5-hexene-4-yl acetate (1.3 g, 4.3 mmole) and ethyl bromoacetate (0.47 ml, 4.2 mmole) in dry THF (10 ml) was added dropwise to a vigorously stirred slurry of activated zinc dust (490 mg, 7.5 mmole), cuprous bromide (29 mg, 0.2 mmole), diethylaluminum chloride (25% solution in toluene; 1.72 ml, 4.3 mmole) and dry THF (5 ml) under N2 at 20° C. Stirring was continued for 5 hours before quenching with pyridine (3.5 ml). After the addition of water (50 ml) the mixture was extracted with ether (3×80 ml). The combined ether extracts were washed with 1 N HCl (2×25 ml), H2O (2×50 ml) and brine, then dried (MgSO4), filtered and evaporated leaving the crude title compound as a pale yellow oil (1.2 g); pmr (CDCl3) δ1.28 (3 H, t), 1.33 (3H, t), 2.10 (3H, s).

Workup

  1. custombefore quenching with pyridine (3.5 ml)
  2. additionAfter the addition of water (50 ml) the mixture
  3. extractionwas extracted with ether (3×80 ml)
  4. washThe combined ether extracts were washed with 1 N HCl (2×25 ml), H2O (2×50 ml) and brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-70e71b7d612e41a19000ff3c86dc976e
Source dataset
uspto-grants-1983_03
Patent number
US04375475

Reaction notes

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