Carbon Dioxide → 3-Dodecyl-5-isoxazole acetic acid

HRID 1938724ノート

反応式

HRID 1938724 の反応式
[CH2:1]([C:13]1[CH:17]=[C:16]([CH3:18])[O:15][N:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C([Li])CCC.[C:24](=[O:26])=[O:25]>O1CCCC1>[CH2:1]([C:13]1[CH:17]=[C:16]([CH2:18][C:24]([OH:26])=[O:25])[O:15][N:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

参加物

5

反応物 3

HCID 280Carbon DioxideHCID 104913863-Dodecyl-5-methylisoxazoleHCID 178418339Butyllithium

生成物 1

HCID 104941103-Dodecyl-5-isoxazole acetic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-75 °C

実験手順

To a cold (-75° C.), stirred suspension of 3-dodecyl-5-methylisoxazole (3.40 g, 0.0135 mol) in dry tetrahydrofuran (900 mL) was added in one portion a 1.6M solution (8.5 mL, 0.014 mol) of n-butyl lithium in hexanes, and the mixture was stirred for 1.5 hours. The mixture was poured onto freshly crushed dry ice and allowed to warm overnight. The mixture was rotoevaporated, and the residue was partitioned between petroleum ether and 0.5M NaOH. The aqueous layer was washed (petroleum ether), acidified with concentrated hydrochloric acid to pH ~1-2, and extracted (CHCl3). The extract was dried (MgSO4) and rotoevaporated to a waxy solid. The solid was recrystallized from toluene to give a white solid; yield 0.65 g (16%); mp 79°-80° C.

後処理

  1. stirringthe mixture was stirred for 1.5 hours
  2. temperatureto warm overnight
  3. customthe residue was partitioned between petroleum ether and 0.5M NaOH
  4. washThe aqueous layer was washed (petroleum ether)
  5. extractionextracted (CHCl3)
  6. dry with materialThe extract was dried (MgSO4)
  7. customThe solid was recrystallized from toluene
  8. customto give a white solid

出典と根拠

ORDレコード
ord-2f876ed9c202492d8ff9656b263a17fb
出典データセット
uspto-grants-1997_12
特許番号
US05693657

反応ノート

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