Cyclododecanecarboxaldehyde → 1-(3-Phenyl-1-propenyl)cyclododecane

HRID 129532

反応式

HRID 129532 の反応式
[Br-].[C:2]1([CH2:8][CH2:9][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([Li])CCC.[CH:34]1([CH:46]=O)[CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]1>CCOCC>[C:2]1([CH2:8][CH:9]=[CH:46][CH:34]2[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45]2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

反応物 3

HCID 78737CyclododecanecarboxaldehydeHCID 10863251Phenethyltriphenylphosphonium bromideHCID 178418339Butyllithium

生成物 1

HCID 544717161-(3-Phenyl-1-propenyl)cyclododecane収率 88.2%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

To 11.4 g (25.5 mmol) of phenylethyl triphenylphosphonium bromide in 50 mL of dry ether at 0° C. is added 10.2 mL (25.5 mmol) of 2.5M butyllithium. The suspension is stirred at 0° C. for 1 hour followed by the addition of 5.0 g (25.5 mmol) of cyclododecane carboxaldehyde. The mixture is stirred at room temperature for 3 hours after which time no starting material is evident by TLC. The reaction mixture is quenched with 1N HCl. The layers are separated and the aqueous layer is washed twice with ethyl ether. The combined organic layers are dried over a MgSO4 and the ether is evaporated. The residue is flash chromatographed on silica gel using hexanes to give 6.4 g of a colorless oil: NMR (CDCl3) δ 1.0-1.6 (m, 10H), 2.6 (m, 1H), 3.4 (d, 2H, J=8 Hz,), 5.3 (t, 1H, J=7 Hz), 5.45 (q, 1H, J=7 Hz), 7.2 ppm (m, 5

後処理

  1. stirringThe mixture is stirred at room temperature for 3 hours after which time no starting material
  2. customThe reaction mixture is quenched with 1N HCl
  3. customThe layers are separated
  4. washthe aqueous layer is washed twice with ethyl ether
  5. dry with materialThe combined organic layers are dried over a MgSO4
  6. customthe ether is evaporated
  7. customchromatographed on silica gel

出典と根拠

ORDレコード
ord-c1a0464607584b3bbe40ecd0acae5021
出典データセット
uspto-grants-1995_11
特許番号
US05468774

関連ノート

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