Benzyl Alcohol → Benzyl azepane-3-carboxylate

HRID 463515ノート

反応式

HRID 463515 の反応式
[C:1]([CH:4]1[CH2:10][CH2:9][CH2:8][CH2:7][NH:6][CH2:5]1)([OH:3])=[O:2].S(Cl)(Cl)=O.CCOCC.[CH2:20](O)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH2:20]([O:2][C:1]([CH:4]1[CH2:10][CH2:9][CH2:8][CH2:7][NH:6][CH2:5]1)=[O:3])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

参加物

5

反応物 4

HCID 244Benzyl AlcoholHCID 3283Diethyl EtherHCID 24386Thionyl ChlorideHCID 13457776Azepane-3-carboxylic acid

生成物 1

HCID 13457777Benzyl azepane-3-carboxylate

実験手順

Suspend 1.15 g 3-carboxyperhydroazepine [P. Krogsgaard-Larsen et al., Acta Chem. Scand., B32, 327 (1978)] in 8 ml benzyl alcohol. Cool the mixture to 0° and add 1 ml thionyl chloride. Stir the mixture at room temperature for 48 hours, then add it dropwise to 300 ml ether with vigorous stirring. Decant the ether and dissolve the residue in H2O. Wash the aqueous solution with ether, then make it to pH 12 and extract with ethyl acetate. Dry the extracts and concentrate in vacuo to obtain 3-benzyloxycarbonylperhydroazepine.

後処理

  1. temperatureCool the mixture to 0°
  2. customDecant the ether
  3. dissolutiondissolve the residue in H2O
  4. washWash the aqueous solution with ether
  5. extractionextract with ethyl acetate
  6. customDry the extracts
  7. concentrationconcentrate in vacuo

出典と根拠

ORDレコード
ord-6b5aae4b46d1497fbcd80a8dc76c7a03
出典データセット
uspto-grants-1985_05
特許番号
US04520021

反応ノート

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