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

HRID 2078503Notes

Reaction equation

HRID 2078503 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) δ 2.56 (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-ecaca7b821354227b64e33806f4d9c29
Source dataset
uspto-grants-2011_04
Patent number
US07928255B2

Reaction notes

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