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Sodium Bicarbonate → HCID 53794764、化合物

HRID 1721905
ノート
印刷プレビュー

反応式

HRID 1721905 の反応式
[Br-].[C:2]1([PH+](C2C=CC=CC=2)C2C=CC=CC=2)[CH:7]=CC=C[CH:3]=1.C([Li])CCC.[C:26]1([CH2:32][O:33][C:34]2[CH:35]=[C:36]([CH:39]=[C:40]([O:42][CH2:43][C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)[CH:41]=2)[CH:37]=O)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.C(=O)(O)[O-:51].[Na+]>C1COCC1.O.Cl>[C:44]1([CH2:43][O:42][C:40]2[CH:39]=[C:36]([CH:37]=[CH:3][CH2:2][CH2:7][OH:51])[CH:35]=[C:34]([O:33][CH2:32][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[CH:41]=2)[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1
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

8

反応物 4

HCID 516892Sodium BicarbonateHCID 517696Phosphine, triphenyl-, hydrobromideHCID 5613513,5-DibenzyloxybenzaldehydeHCID 178418339Butyllithium

生成物 1

HCID 53794764HCID 53794764、化合物

試薬・触媒・溶媒 3

HCID 313Hydrochloric Acid溶媒
HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
0 °C

実験手順

A stirred suspension of [3-(1-methoxy)-1-methylethoxy)propyl](triphenylphosphonium)bromide (4 g) in dry THF (25 ml) at 0° C. was heated with butyl lithium (5.28 ml) and the mixture stirred at 0° C. for 10 min. 3,5-Bis(phenylmethoxy)benzaldehyde (2.24 g) in dry THF (15 ml) was added and the mixture stirred for a further 45 min at room temperature under nitrogen, diluted with ER (100 ml) and filtered through silica (20 g) twice. The filtrate was evaporated in vacuo to give a yellow oil which was dissolved in a mixture of THF (50 ml), water (5 ml) and 2M hydrochloric acid (1 ml) and left at room temperature for 30 min. The mixture was basified with sodium bicarbonate solution and extracted with ER (200 ml). The organic phase was washed with water (150 ml), brine (100 ml), dried and evaporated in vacuo to give a yellow oil. Purification by FCC eluting with ER-CX (3:2) gave a colourless oil (1.48 g). T.l.c. (ER-CX 3:1) Rf 0.26

後処理

  1. stirringthe mixture stirred for a further 45 min at room temperature under nitrogen
  2. additiondiluted with ER (100 ml)
  3. filtrationfiltered through silica (20 g) twice
  4. customThe filtrate was evaporated in vacuo
  5. customto give a yellow oil which
  6. waitleft at room temperature for 30 min
  7. extractionextracted with ER (200 ml)
  8. washThe organic phase was washed with water (150 ml), brine (100 ml)
  9. customdried
  10. customevaporated in vacuo
  11. customto give a yellow oil
  12. customPurification by FCC
  13. washeluting with ER-CX (3:2)

出典と根拠

ORDレコード
ord-7fe34270ece14d1c9dd2d0c266604326
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04853382

反応ノート

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