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Hydrochloric Acid → 4-Methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride

HRID 74569
ノート
印刷プレビュー

反応式

HRID 74569 の反応式
[H][H].[CH3:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[N:6][CH:5]=1.[ClH:14]>CO.[Pt](=O)=O>[ClH:14].[CH3:3][CH:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][NH:6][CH2:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 640939Isoquinoline, 4-methyl-HCID 178418361HCID 178418361、化合物

生成物 1

HCID 137389354-Methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride

試薬・触媒・溶媒 2

HCID 345198Adams' catalyst触媒HCID 887Methanol溶媒

実験手順

In a hydrogen atmosphere 0.50 g (3.5 mmol) 4-methyl-isoquinoline, 50 mg platinum dioxide in 50 mL methanol and 3.5 mL 1M aqueous hydrochloric acid solution were hydrogenated at RT and 3 bar for 4 h. After removal of the catalyst by suction filtering the reaction mixture was evaporated down. A mixture of educt and product was obtained, which was reacted further without any further purification.

後処理

  1. customwere hydrogenated at RT
  2. customAfter removal of the catalyst by suction
  3. filtrationfiltering the reaction mixture
  4. customwas evaporated down
  5. additionA mixture of educt
  6. customproduct was obtained
  7. customwhich was reacted further without any further purification

出典と根拠

ORDレコード
ord-1321a3bcf39b40b99dddf7a6e3b25de7
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08829006B2

反応ノート

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