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Hydrochloric Acid → 5-Chloro-3-(2-tritylamino-3-hydroxypropoxy)-1,2-benzoisoxazole

HRID 1901600
ノート
印刷プレビュー

反応式

HRID 1901600 の反応式
[C:1](Cl)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:21][CH:22]([CH2:35][OH:36])[CH2:23][O:24][C:25]1[C:29]2[CH:30]=[C:31]([Cl:34])[CH:32]=[CH:33][C:28]=2[O:27][N:26]=1.C(N(CC)CC)C.Cl>CN(C)C=O.C(OCC)(=O)C>[Cl:34][C:31]1[CH:32]=[CH:33][C:28]2[O:27][N:26]=[C:25]([O:24][CH2:23][CH:22]([NH:21][C:1]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH2:35][OH:36])[C:29]=2[CH:30]=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 4

HCID 313Hydrochloric AcidHCID 6456Trityl chlorideHCID 8471TriethylamineHCID 153825803-(2-Amino-3-hydroxypropoxy)-5-chloro-1,2-benzoisoxazole

生成物 1

HCID 233684925-Chloro-3-(2-tritylamino-3-hydroxypropoxy)-1,2-benzoisoxazole

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

実験手順

A solution of 5.58 g of trityl chloride in 6 ml of N,N-dimethylformamide is added to a solution of 4.85 g of 3-(2-amino-3-hydroxypropoxy)-5-chloro-1,2-benzoisoxazole and 2.02 g of triethylamine in 12 ml of N,N-dimethylformamide at -40° to -30° C., and they are subjected to reaction at the same temperature for 30 minutes. Subsequently, ice water and ethyl acetate are added to the reaction mixture and the pH is adjusted to 2 with 2N hydrochloric acid. The organic layer is separated, and the separated organic layer is washed with a saturated saline solution and dried over anhydrous magnesium sulfate, after which the solvent is removed by distillation under reduced pressure. The residue obtained is crystallized from n-hexane and the crystals are collected by filtration, to obtain 7.28 g of colorless, crystalline 5-chloro-3-(2-tritylamino-3-hydroxypropoxy)-1,2-benzoisoxazole having a melting point of 142°-144° C.

後処理

  1. customthey are subjected to reaction at the same temperature for 30 minutes
  2. customThe organic layer is separated
  3. washthe separated organic layer is washed with a saturated saline solution
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customafter which the solvent is removed by distillation under reduced pressure
  6. customThe residue obtained
  7. customis crystallized from n-hexane
  8. filtrationthe crystals are collected by filtration

出典と根拠

ORDレコード
ord-ca787c46f3524ff7b57cd5a82caa3689
出典データセット
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05578627

反応ノート

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