Tetrahydrofuran → HCID 66936654, compound

HRID 1367786Notes

Reaction equation

HRID 1367786 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9]([CH3:12])([CH3:11])OC[C:6]=2[CH:13]=1.C([Li])CCC.CN(OC)[C:21](=[O:23])[CH3:22].C1C[O:29][CH2:28]C1>C(OCC)(=O)C>[C:21]([C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9]([CH3:11])([CH3:12])[CH2:28][O:29][C:6]=2[CH:13]=1)(=[O:23])[CH3:22]

Participants

6

Reactant 4

HCID 8028TetrahydrofuranHCID 537505N-Methoxy-N-methylacetamideHCID 145203386-Bromo-2,2-dimethyl-4H-benzo[d][1,3]dioxineHCID 178418339Butyllithium

Product 1

HCID 66936654HCID 66936654, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

To the product of step (a) (110 g, 0.46 mol) in 1.0 L of THF at −78° C. was added 236 mL (0.51 mol) of 2.14 M n-butyllithium in hexanes via a dropping funnel. After 30 minutes, N-methyl-N-methoxy acetamide (71 g, 0.69 mol, available from TCI) was added. After 2 hours, the reaction mixture was quenched with water, diluted with 2.0 L of 1.0 M aqueous phosphate buffer (pH=7.0) and extracted once with diethyl ether. The diethyl ether phase was washed once with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give a light orange oil. The oil was dissolved in a minimum volume of ethyl acetate, diluted with hexanes, and to give the title compound as a crystalline solid.

Workup

  1. waitAfter 2 hours
  2. customthe reaction mixture was quenched with water
  3. additiondiluted with 2.0 L of 1.0 M aqueous phosphate buffer (pH=7.0)
  4. extractionextracted once with diethyl ether
  5. washThe diethyl ether phase was washed once with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto give a light orange oil

Sources & evidence

ORD record
ord-17c7be3f08484ddb90f80314788f2e9e
Source dataset
uspto-grants-2011_02
Patent number
US07893256B2

Reaction notes

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