Dichloromethane → HCID 11776281、化合物

HRID 257434ノート

反応式

HRID 257434 の反応式
[CH:1]1([O:7][CH2:8][CH2:9][CH2:10][OH:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.ClCCl.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>C(N(CC)CC)C>[CH3:15][S:16]([O:11][CH2:10][CH2:9][CH2:8][O:7][CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)(=[O:18])=[O:17]

参加物

5

反応物 3

HCID 6344DichloromethaneHCID 31297Methanesulfonyl chlorideHCID 100348783-(Cyclohexyloxy)propan-1-ol

生成物 1

HCID 11776281HCID 11776281、化合物収率 57.8%

試薬・触媒・溶媒 1

HCID 8471Triethylamine溶媒

実験手順

To a solution of 10 parts of 3-(cyclohexyloxy)-1-propanol in 160 parts of dichloromethane there were added 11.2 parts of N,N-diethylethanamine and dropwise 8.14 parts of methanesulfonyl chloride. The whole was stirred for 9 hours at room temperature. The reaction mixture was washed with Na2CO3 (aq.) and water and was then dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 99:1). The eluent of the desired fraction was evaporated and the residue was co-evaporated with methylbenzene. The product was filtered off and dried, yielding 8.6 parts (57.8%) of 3-(cyclohexyloxy)-1-propanol methanesulfonate (ester) (interm. 21).

後処理

  1. washThe reaction mixture was washed with Na2CO3 (aq.) and water
  2. customwas then dried
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 99:1)
  6. customThe eluent of the desired fraction was evaporated
  7. filtrationThe product was filtered off
  8. customdried

出典と根拠

ORDレコード
ord-56e0b7c361dd4e79bd420a70a1e7502c
出典データセット
uspto-grants-1993_11
特許番号
US05262418

反応ノート

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