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Lithium Chloride → Tert-butyl 4-(hydroxymethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

HRID 227566
ノート
印刷プレビュー

反応式

HRID 227566 の反応式
[BH4-].[Na+].[Li+].[Cl-].C[O:6][C:7]([CH:9]1[CH2:13][O:12][C:11]([CH3:15])([CH3:14])[N:10]1[C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])=O>CCO.C1COCC1>[C:19]([O:18][C:16]([N:10]1[CH:9]([CH2:7][OH:6])[CH2:13][O:12][C:11]1([CH3:15])[CH3:14])=[O:17])([CH3:22])([CH3:21])[CH3:20]
参加物反応条件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 433294Lithium ChlorideHCID 4311764Sodium borohydrideHCID 51384973-tert-Butyl 4-methyl 2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylate

生成物 1

HCID 14409442Tert-butyl 4-(hydroxymethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

To a mixture of NaBH4 (2.247 g, 59.08 mmol) and LiCl (2.505 g, 59.08 mmol) in EtOH (42 mL), stirring under nitrogen at 0° C., was added (35) (7.659 g, 29.54 mmol) in THF (30 mL) dropwise. This mixture was allowed to warn to room temperature and continued stirring for 48 hours. The precipitate was filtered and washed with ethanol. The washings were concentrated and extracted with EtOAc. The organic layer was then washed with brine and dried over anhydrous Na2SO4. Column chromatography on SiO2 (1:1 EtOAc/Hexanes) was utilized to purify 6.101 g (89%) of the title compound as a white solid.

後処理

  1. customto warn to room temperature
  2. stirringcontinued stirring for 48 hours
  3. filtrationThe precipitate was filtered
  4. washwashed with ethanol
  5. concentrationThe washings were concentrated
  6. extractionextracted with EtOAc
  7. washThe organic layer was then washed with brine
  8. dry with materialdried over anhydrous Na2SO4
  9. customto purify 6.101 g (89%) of the title compound as a white solid

出典と根拠

ORDレコード
ord-018d7a518f2c4a5cabd26bc13a623460
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07560477B2

反応ノート

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