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

HRID 1961325

Reaction equation

HRID 1961325 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-3f8425d7fec442ba9e0a39cde08a5cc1
Source dataset
uspto-grants-2013_04
Patent number
US08410158B2

Linked notes

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