反応 #3081

ord-bc41cd91f23e45a6ab06f2b380bb0c6e

反応方程式

O=C(O)CCCCC(O)CCCl
(+)-8-chloro-6-hydroxy-octanoic acid
c1ccncc1
pyridine
O=S(Cl)Cl
thionyl chloride
O=C(O)CCCCC(Cl)CCCl
(-)-6,8-dichloro-octanoic acid

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The mixture was then refluxed for 1 hour
  2. 2
    その他The organic phase was then removed
  3. 3
    洗浄washed with 20 ml water
  4. 4
    その他The aqueous phase was then removed
  5. 5
    抽出extracted twice with 20 ml diethylether
  6. 6
    乾燥The combined ether extracts were dried over magnesium sulfate
  7. 7
    その他After that, the solvent was evaporated under vacuum

実験手順

To a solution of 2.4 g (12.3 mmoles) of (+)-8-chloro-6-hydroxy-octanoic acid (+)-(VI) and 0.05 g (0.6 mmoles) of pyridine in 30 ml toluene, 3.3 g (27.7 mmoles) of thionyl chloride were added slowly. The mixture was then refluxed for 1 hour. The reaction mixture was cooled to room temperature and added to 50 ml ice water. The organic phase was then removed, washed with 20 ml water and stirred for 4 hours with 30 ml of 2N NaOH. The aqueous phase was then removed, adjusted to a pH of 1 with 3N HCl and extracted twice with 20 ml diethylether. The combined ether extracts were dried over magnesium sulfate. After that, the solvent was evaporated under vacuum. (-)-6,8-dichloro-octanoic acid (-)-(VII) was obtained in a yield of 2.1 g (80% of the theoretical yield). [α]D20 =-30.6° (c=1; benzene).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05731448uspto-grants-1998_03