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Ammonium Chloride → HCID 58609721、化合物

HRID 1820614
ノート
印刷プレビュー

反応式

HRID 1820614 の反応式
[Si:1]([O:18][CH2:19][C:20]([O:22]CC)=O)([C:14]([CH3:17])([CH3:16])[CH3:15])([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.[CH2:25]([Mg]Br)[CH:26]([CH3:28])[CH3:27].[Cl-].[NH4+]>O1CCCC1.CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Ti+4]>[Si:1]([O:18][CH2:19][C:20]1([OH:22])[CH2:25][C:26]1([CH3:28])[CH3:27])([C:14]([CH3:15])([CH3:17])[CH3:16])([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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 25517Ammonium ChlorideHCID 59464758(tert-Butyl-diphenyl-silanyloxy)-acetic acid ethyl esterHCID 178418816HCID 178418816、化合物

生成物 1

HCID 58609721HCID 58609721、化合物

試薬・触媒・溶媒 2

HCID 11026Titanium isopropoxide触媒HCID 8028Tetrahydrofuran
溶媒
2 回

実験手順

According to the description in a reference (see: Syn. Lett. 07, 1053-1054, 1999), the title compound was prepared as follows. 10 g (29 mmole) of ethyl 2-{[t-butyl(diphenyl)silyl]oxy}acetate was dissolved in 100 ml of tetrahydrofuran (THF) and 6.0 ml of titaniumtetraisopropoxide was added thereto. To the mixture was slowly added 37 ml of isobutylmagnesiumbromide (2.0M in THF) at −10° C., and the reaction solution was stirred for 12 hours at room temperature. 50 ml of saturated ammonium chloride was added to stop the reaction. The tetrahydrofuran (THF) used as a solvent was removed by distillation under reduced pressure, and the reaction mixture was extracted twice with 500 ml of n-hexane. The n-hexane extract was distilled under reduced pressure and purified by silica gel column to give 5.0 g of the title compound.

後処理

  1. customthe title compound was prepared
  2. customat −10° C.
  3. customthe reaction
  4. customwas removed by distillation under reduced pressure
  5. extractionthe reaction mixture was extracted twice with 500 ml of n-hexane
  6. extractionThe n-hexane extract
  7. distillationwas distilled under reduced pressure
  8. custompurified by silica gel column

出典と根拠

ORDレコード
ord-85ad3bef731648f5966dfc9d2bde8d77
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07605147B2

反応ノート

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