تفاعل #969843

ord-c54f375f643f4e4da28943cfdc5096d9

معادلة التفاعل

O=C(O)Cc1cccs1
thiolacetic acid
CCN(C(C)C)C(C)C
DIPEA
C1CCOC1
THF
COC(=O)C(Br)CCBr
methyl 2,4-dibromobutanoate
C1CCOC1
THF
COC(=O)C(CCBr)SC(C)=O
title compound
المردود 96.0%
COC(=O)C(CCBr)SC(C)=O
Methyl 2-(acetylthio)-4-bromobutanoate
المردود 96.0%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
-20°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAIT0° C. for 2 hours under Ar
  2. 2
    تركيزthe mixture was concentrated
  3. 3
    workup.ADDITIONdiluted with EtAc/Hexane
  4. 4
    غسيلwashed with 1.0 M NaH2PO4
  5. 5
    تجفيفdried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    أخرىevaporated
  8. 8
    أخرىSiO2 chromatographic purification (1:12 to 1:10 EtAc/Hexane)

الإجراء التجريبي

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)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08236319B2uspto-grants-2012_08