Tetrahydrofuran → Methyl 2-(acetylthio)-4-bromobutanoate

HRID 1914435Notes

Reaction equation

HRID 1914435 reaction equation
Br[CH:2]([CH2:7][CH2:8][Br:9])[C:3]([O:5][CH3:6])=[O:4].[S:10]1C=CC=C1CC(O)=O.CCN(C(C)C)C(C)C.C1C[O:31][CH2:30][CH2:29]1>>[C:30]([S:10][CH:2]([CH2:7][CH2:8][Br:9])[C:3]([O:5][CH3:6])=[O:4])(=[O:31])[CH3:29]

Participants

5

Conditions

Temperature
-20 °C

Procedure

10.0 g (38.4 mmol) of methyl 2,4-dibromobutanoate in 100 ml of dry THF at 20° C. was added drop wise the mixture of 2.75 ml (38.5 mmol) of thiolacetic acid in 8.5 ml (48.9 mmol) of DIPEA and 50 ml of dry THF in 1.5 hour. After stirring overnight at −20° C. then 0° C. for 2 hours under Ar, the mixture was concentrated, diluted with EtAc/Hexane, washed with 1.0 M NaH2PO4, dried over MgSO4, filtered, evaporated, and SiO2 chromatographic purification (1:12 to 1:10 EtAc/Hexane) to afford 9.5 g (96%) of the title compound. 1H NMR (CDCl3) 4.38 (1H, t, J=7.1 Hz), 3.74 (s, 3H), 3.40 (m, 2H), 2.57˜2.47 (m, 1H), 2.37 (s, 3H), 2.36˜2.21 (m, 1H); 13C NMR 193.24, 171.36, 53.15, 44.45, 34.67, 30.46, 29.46; MS m/z+ 276.9 (M+Na), 278.9 (M+2+Na)

Workup

  1. wait0° C. for 2 hours under Ar
  2. concentrationthe mixture was concentrated
  3. additiondiluted with EtAc/Hexane
  4. washwashed with 1.0 M NaH2PO4
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated
  8. customSiO2 chromatographic purification (1:12 to 1:10 EtAc/Hexane)

Sources & evidence

ORD record
ord-fbcf9c89ac344093a542b6a82900e8d4
Source dataset
uspto-grants-2013_12
Patent number
US08613930B2

Reaction notes

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