2-Chlorooctane → Methyl 4-Bromo-5-chloro-2-furoate

HRID 1845695Notes

Reaction equation

HRID 1845695 reaction equation
C([Mg][Cl:5])(C)C.[Br:6][C:7]1[CH:8]=[C:9]([C:13]([O:15][CH3:16])=[O:14])[O:10][C:11]=1Br.C(C(Cl)C)CCCCC>O1CCCC1>[Br:6][C:7]1[CH:8]=[C:9]([C:13]([O:15][CH3:16])=[O:14])[O:10][C:11]=1[Cl:5]

Participants

5

Conditions

Temperature
-78 °C

Procedure

Isopropylmagnesium chloride (1.20 ml, 2.40 mmol) was added dropwise to a solution of methyl 4,5-dibromo-2-furancarboxylate (568 mg, 2.0 mmol) in Tetrahydrofuran (THF) (16 ml) at 0° C. The resulting mixture was stirred at this temperature for 30 min and then cooled to −78° C. A solution of hexylchloroethane (568 mg, 2.401 mmol) in THF (1 mL) was added dropwise, and the resulting mixture was stirred at this temperature for 1 hr. The reaction was quenched with addition of NH4Cl (sat. aq) and the resulting mixture was stirred at rt overnight. Ether and water were added and the aqueous layer was discarded. The organic layer was washed with brine, dried (Na2SO4) and concentrated to give 0.34 g of the product containing its isopropyl ester.

Workup

  1. stirringthe resulting mixture was stirred at this temperature for 1 hr
  2. customThe reaction was quenched with addition of NH4Cl (sat. aq)
  3. stirringthe resulting mixture was stirred at rt overnight
  4. additionEther and water were added
  5. washThe organic layer was washed with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-4b64e38fd5a04977b2a9680fcf874624
Source dataset
uspto-grants-2015_02
Patent number
US08946278B2

Reaction notes

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