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Diethyl Oxalate → Ethyl 3-methyl-2,4-dioxohexanoate

HRID 2388246
ノート
印刷プレビュー

反応式

HRID 2388246 の反応式
[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[CH3:11][CH2:12][C:13](=[O:16])[CH2:14][CH3:15].[C:17]([O:24][CH2:25][CH3:26])(=[O:23])[C:18]([O:20]CC)=O>CCOCC>[CH2:25]([O:24][C:17](=[O:23])[C:18](=[O:20])[CH:12]([CH3:11])[C:13](=[O:16])[CH2:14][CH3:15])[CH3:26]
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

5

反応物 3

HCID 7268Diethyl OxalateHCID 7288Ethyl ketoneHCID 2733832Lithium hexamethyldisilazane

生成物 1

HCID 3017239Ethyl 3-methyl-2,4-dioxohexanoate収率 95.8%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
-78 °C

実験手順

LHMDS solution (35.7 mL, 35.7 mmol, 1M in hexanes) was added to 200 mL of diethyl ether and the mixture was cooled to −78° C. 3-Pentanone (3.8 mL, 35.7 mmol) dissolved in 50 mL of ether was added dropwise, and the resulting mixture was stirred at −78° C. for 1 h. Diethyl oxalate (5.3 mL, 39.3 mmol) was added dropwise, and the cooling bath was removed and the mixture was allowed to come to room temperature. After the mixture was stirred for 16 h, the resulting precipitate was isolated by filtration. The solid was partitioned between CH2Cl2 (150 mL) and 1M hydrochloric acid (100 mL), and the aqueous layer was extracted with additional CH2Cl2. The combined organic layer was dried over MgSO4 and concentrated to give 6.37 g of the title compound. MS: (−) m/z 185.28 (M−1).

後処理

  1. additionwas added dropwise
  2. customthe cooling bath was removed
  3. customto come to room temperature
  4. stirringAfter the mixture was stirred for 16 h
  5. customthe resulting precipitate was isolated by filtration
  6. customThe solid was partitioned between CH2Cl2 (150 mL) and 1M hydrochloric acid (100 mL)
  7. extractionthe aqueous layer was extracted with additional CH2Cl2
  8. dry with materialThe combined organic layer was dried over MgSO4
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-ffef7cd658594e76ae065a3c8c8da0ea
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08269008B2

反応ノート

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