Pyridine → 6-Chloro-8-methylthiooctanoic acid ethyl ester

HRID 247180노트

반응식

HRID 247180 반응식
S(Cl)([Cl:3])=O.[CH2:5]([O:7][C:8](=[S:18])[CH2:9][CH2:10][CH2:11][CH2:12][CH:13](O)[CH2:14][CH2:15][CH3:16])[CH3:6].N1C=CC=CC=1>ClCCl>[CH2:5]([O:7][C:8](=[S:18])[CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([Cl:3])[CH2:14][CH2:15][CH3:16])[CH3:6]

참가 물질

5

반응물 3

HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 545259706-Hydroxy-8-methylthiooctanoic acid ethyl ester

생성물 1

HCID 536593926-Chloro-8-methylthiooctanoic acid ethyl ester수율 89.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

89.25 grams (0.7 mole) of thionyl chloride at +5° C. were slowly dropped into a solution of 137.0 grams (0.59 mole) of 6-hydroxy-8-methylthiooctanoic acid ethyl ester (VIb) and 1 ml of pyridine in 300 ml of dichloromethane. After stirring for 1 hour at +10° C. the mixture was heated for 3 hours at reflux and subsequently concentrated in a vacuum. The residue was treated with 200 ml of water and extracted with dichloromethane. After drying the combined extracts with sodium sulfate the solvent was removed in a vacuum. By fractional distillation there were obtained 125.1 grams (84% of theory) of 6-chloro-8-methylthiooctanoic acid ethyl ester as a colorless oil having a boiling point of 135° C. to 145° C. at 1 mbar.

후처리

  1. temperaturewas heated for 3 hours
  2. temperatureat reflux
  3. concentrationsubsequently concentrated in a vacuum
  4. additionThe residue was treated with 200 ml of water
  5. extractionextracted with dichloromethane
  6. dry with materialAfter drying the combined extracts with sodium sulfate the solvent
  7. customwas removed in a vacuum
  8. distillationBy fractional distillation there

출처 및 근거

ORD 기록
ord-46bb3864cde948f0a53326263fda093b
출처 데이터셋
uspto-grants-1987_11
특허 번호
US04705867

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