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1,3-Propanediol → HCID 19789726、化合物

HRID 1655928
ノート
印刷プレビュー

反応式

HRID 1655928 の反応式
[CH2:1]([OH:5])[CH2:2][CH2:3][OH:4].[H-].[Na+].Cl[CH2:9][O:10][CH:11]([CH3:13])[CH3:12]>O1CCCC1>[CH:11]([O:10][CH2:9][O:4][CH2:3][CH2:2][CH2:1][OH:5])([CH3:13])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 104421,3-PropanediolHCID 24758Sodium hydrideHCID 124317162-(Chloromethoxy)propane

生成物 1

HCID 19789726HCID 19789726、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 1,3-propanediol (19.4 g, 255 mmol) in dry tetrahydrofuran (100 ml) under nitrogen at 0°-5° C. was treated with sodium hydride (2.04 g, 85 mmol) and stirred for 1 hour. Chloromethylisopropyl ether (9 g, 83 mmol) in dry tetrahydrofuran (15 ml) was added over 15 min. Stirring was continued for a further 2 hours. The reaction mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica eluting with dichloromethane:methanol (97:4) to give the title compound as a colourless oil. (5.3 g, 44%). νmax (Film) 3400, 2910, 2860, 2805, 2760, 1460, 1440, 1425, 1410 and 1380 cm-1 ; δH (CDCl3) 1.17 (3H, s, CH3), 1.20 (3H, s,CH3), 1.84 (2H, quintet, J=6 Hz CH2CH2CH2), 2.3 (1H, br s, D2O exchangeable OH), 3.72 (2H, t, J=6 Hz, CH2OCH2OCH(CH3)2) 3.76 (2H, t, J=6 Hz,CH2ON), 3.86 (1H, m, CH(CH3)2), 4.70 (2H, s, OCH2O).

後処理

  1. stirringStirring
  2. waitwas continued for a further 2 hours
  3. filtrationThe reaction mixture was filtered
  4. customthe filtrate was evaporated in vacuo
  5. customThe residue was purified by column chromatography on silica eluting with dichloromethane:methanol (97:4)

出典と根拠

ORDレコード
ord-9ea29e242d344fcca803a2db40cd66a7
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05252575

反応ノート

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