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Methyl p-toluenesulfonate → 2,2-Dimethyl-3-hydroxymethyl-1,2,3,4-tetrahydroisoquinolinium p-toluenesulfonate

HRID 1088562
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반응식

HRID 1088562 반응식
[CH3:1][N:2]1[CH:11]([CH2:12][OH:13])[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3]1.[C:14]1([CH3:25])[CH:19]=[CH:18][C:17]([S:20]([O:23]C)(=[O:22])=[O:21])=[CH:16][CH:15]=1>CC(C)=O>[C:14]1([CH3:25])[CH:15]=[CH:16][C:17]([S:20]([O-:23])(=[O:21])=[O:22])=[CH:18][CH:19]=1.[CH3:1][N+:2]1([CH3:14])[CH:11]([CH2:12][OH:13])[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3]1
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참가 물질

4

반응물 2

HCID 6645Methyl p-toluenesulfonateHCID 589740(2-Methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

생성물 1

HCID 150522362,2-Dimethyl-3-hydroxymethyl-1,2,3,4-tetrahydroisoquinolinium p-toluenesulfonate수율 144%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In 12 ml of acetone was dissolved 887 mg of 2-methyl-1,2,3,4-tetrahydro-3-isoquinolinemethanol, and 932 mg of methyl p-toluenesulfonate was added dropwise to the resulting solution. The mixture was stirred at room temperature for 3 hours to precipitate crystals. The crystals were collected by filtration, washed with acetone and dried under reduced pressure to give 1.31 g of the desired compound.

후처리

  1. additionwas added dropwise to the resulting solution
  2. customto precipitate crystals
  3. filtrationThe crystals were collected by filtration
  4. washwashed with acetone
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-dd7d94056c554f6c9ba57702b4941e96
출처 데이터셋
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04962096

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