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Hydrochloric Acid → 1'-benzyl-6-ethylspiro[isobenzofuran-1(3H),4'-piperidine]-3-one hydrochloride

HRID 392806
ノート
印刷プレビュー

反応式

HRID 392806 の反応式
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10]CC(C)(C)N=2)=[CH:5][CH:4]=1)[CH3:2].CCCCCC.C([Li])CCC.[CH2:27]([N:34]1[CH2:39][CH2:38][C:37](=[O:40])[CH2:36][CH2:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[ClH:41].[OH-].[Na+]>O1CCCC1>[ClH:41].[CH2:27]([N:34]1[CH2:39][CH2:38][C:37]2([C:7]3[C:6](=[CH:5][CH:4]=[C:3]([CH2:1][CH3:2])[CH:8]=3)[C:9](=[O:10])[O:40]2)[CH2:36][CH2:35]1)[C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 192201-Benzyl-4-piperidoneHCID 128725592-(4-Ethylphenyl)-4,4-dimethyl-2-oxazolineHCID 178418244HCID 178418244、化合物

生成物 1

HCID 226607251'-benzyl-6-ethylspiro[isobenzofuran-1(3H),4'-piperidine]-3-one hydrochloride

試薬・触媒・溶媒

1
HCID 8028Tetrahydrofuran溶媒

実験手順

Under a nitrogen atmosphere, a solution of 2-(4-ethylphenyl)-4,4-dimethyl-2-oxazoline (1.15 g) in anhydrous tetrahydrofuran (100 mL) was cooled to −78° C. To this solution was added 1.5 M butyl lithium hexane solution (4.53 mL). After being stirred for 1 hour, 1-benzyl-4-piperidone (1.05 mL) was added dropwise. After the reaction temperature was allowed to rise up to room temperature, 2N hydrochloric acid was added to the reaction mixture to make the mixture acidic. The whole was refluxed for 2 hours. After cooling, sodium hydroxide aqueous solution was added to make the reaction mixture basic. The mixture was extracted with ethyl ether. The organic layer was washed with saturated saline solution and then dried over anhydrous Na2SO4. The concentration of the organic solvent left a residue, which was purified by column chromatography on silica gel (hexane/ethyl acetate/=3/2) to give the subject compound (409 mg).

後処理

  1. customto rise up to room temperature
  2. temperatureThe whole was refluxed for 2 hours
  3. temperatureAfter cooling
  4. extractionThe mixture was extracted with ethyl ether
  5. washThe organic layer was washed with saturated saline solution
  6. dry with materialdried over anhydrous Na2SO4
  7. waitThe concentration of the organic solvent left a residue, which
  8. customwas purified by column chromatography on silica gel (hexane/ethyl acetate/=3/2)

出典と根拠

ORDレコード
ord-e8321f610e0a4d0583fed708ad8b4ad9
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06803372B2

反応ノート

読み込み中…

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