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Ammonium Chloride → Ethyl 8-acetyl-12-(acetyloxy)-8-methylheptadecanoate

HRID 1730226
ノート
印刷プレビュー

反応式

HRID 1730226 の反応式
[I-].[CH3:2][Li].[C:4]([C:7](Br)([CH2:19][CH2:20][CH2:21][CH:22]([O:28][C:29](=[O:31])[CH3:30])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])(=[O:6])[CH3:5].[Cl-].[NH4+]>CCOCC>[C:4]([C:7]([CH3:2])([CH2:19][CH2:20][CH2:21][CH:22]([O:28][C:29](=[O:31])[CH3:30])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])(=[O:6])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 25517Ammonium ChlorideHCID 30165Iodide IonHCID 21397377Ethyl 8-acetyl-12-(acetyloxy)-8-bromoheptadecanoateHCID 178418348HCID 178418348、化合物

生成物 1

HCID 21397375Ethyl 8-acetyl-12-(acetyloxy)-8-methylheptadecanoate

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether
溶媒
2 回

実験手順

Cupruous iodide (7.1 g., 0.037 mole) is suspended in ether (150 ml.) and a 1.66 M solution of methyl lithium in ether (45 ml., 0.075 mole) is added dropwise during 30 minutes. Ethyl 8-acetyl-8-bromo-12-acetoxyheptadecanoate (11.9 g., 0.025 mole) is added dropwise during 30 minutes. The temperature is kept at -4° C to -2° C. during these operations by means of a salt bath. Stirring is continued at this temperature for another 30 minutes; then the mixture is stirred for 2 hours without cooling. The reaction mixture is then treated with 200 ml. of saturated ammonium chloride solution. The organic layer is separated, washed with brine and dried over sodium sulfate. Distillation of the solvent in vacuo leaves the crude product as an orange oil weighing 9.2 g. The product is purified by column chromatography using 250 g. of silica gel and chloroform as the eluant. Ethyl 8-acetyl-8-methyl-12-acetoxyheptadecanoate is obtained as yellow viscous oil.

後処理

  1. customThe temperature is kept at -4° C to -2° C. during these operations by means of a salt bath
  2. stirringthen the mixture is stirred for 2 hours
  3. temperaturewithout cooling
  4. additionThe reaction mixture is then treated with 200 ml
  5. customThe organic layer is separated
  6. washwashed with brine
  7. dry with materialdried over sodium sulfate
  8. distillationDistillation of the solvent in vacuo
  9. customleaves the crude product as an orange oil
  10. customThe product is purified by column chromatography

出典と根拠

ORDレコード
ord-4643de0cbfc3407397c202187cab33fc
出典データセット
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03991087

反応ノート

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