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

HRID 882661

Reaction equation

HRID 882661 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-c54f375f643f4e4da28943cfdc5096d9
Source dataset
uspto-grants-2012_08
Patent number
US08236319B2

Linked notes

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