Methanol → 3-Butyn-2-ol, 1-(4-fluorophenoxy)-, (2S)-

HRID 1671736Notes

Reaction equation

HRID 1671736 reaction equation
[F:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][CH2:7][C@@H:8]([O:11]C(=O)C2C=C([N+]([O-])=O)C=C([N+]([O-])=O)C=2)[C:9]#[CH:10])=[CH:4][CH:3]=1.CO.C([O-])([O-])=O.[K+].[K+]>C1COCC1>[F:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][CH2:7][C@@H:8]([OH:11])[C:9]#[CH:10])=[CH:4][CH:3]=1

Participants

5

Procedure

To a solution of (3S)-4-(4-fluorophenoxy)-3-(3′,5′-dinitrobenzoyl)oxy-1-butyne (10.35 g, 98% ee, 27.6 mmol) in THF (115 mL), was added methanol (115 mL) and K2CO3 (0.58 g). After stirring for 3.5 hours, the reaction mixture was quenched with acetic acid (2 mL). The solvents were evaporated and the resulting slurry was filtered and the solid was washed with ether. The filtrate was concentrated and the filtration/ether wash sequence was repeated. Concentration gave 4.02 g of (3S)-4-(4-fluorophenoxy)-3-hydroxy-1-butyne (98% ee), a compound of formula (BB); 1H NMR (CDCl3) δ2.56 (s, 1H), 4.10 (m, 2H), 4.78 (m, 1H), 6.85 (m, 2H), 7.0 (m, 2H).

Workup

  1. customthe reaction mixture was quenched with acetic acid (2 mL)
  2. customThe solvents were evaporated
  3. filtrationthe resulting slurry was filtered
  4. washthe solid was washed with ether
  5. concentrationThe filtrate was concentrated
  6. filtrationthe filtration/ether
  7. washwash sequence
  8. concentrationConcentration

Sources & evidence

ORD record
ord-707b5123d53c44639222d5d90f80597d
Source dataset
uspto-grants-2011_08
Patent number
US07994346B2

Reaction notes

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