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Acetic Acid → Ethyl 2-(butoxyimino)-4-chloro-3-oxobutanoate

HRID 543940
ノート
印刷プレビュー

反応式

HRID 543940 の反応式
[CH2:1]([O:5][N:6]=[C:7]([C:13](=[O:15])[CH3:14])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:2][CH2:3][CH3:4].S(Cl)([Cl:19])(=O)=O.C(O)(=O)C>O>[CH2:1]([O:5][N:6]=[C:7]([C:13](=[O:15])[CH2:14][Cl:19])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:2][CH2:3][CH3:4]
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 176Acetic AcidHCID 24648Sulfuryl chlorideHCID 53974956Ethyl 2-(butoxyimino)-3-oxobutanoate

生成物 1

HCID 54055311Ethyl 2-(butoxyimino)-4-chloro-3-oxobutanoate収率 92%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of ethyl 2-n-butoxyimino-3-oxobutyrate (syn isomer, 48.8 g.), sulfuryl chloride (31.5 g.) and acetic acid (48.8 ml.) was stirred at 40° C. for 10 minutes and further at room temperature for 5.5 hours. After water (300 ml.) was added to the resultant solution under ice cooling, the solution was extracted with methylene chloride three times. The extract was washed with water, an aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in turn, and dried over magnesium sulfate. The solution was concentrated in vacuo to give ethyl 2-n-butoxyimino-4-chloro-3-oxobutyrate (syn isomer, 52.1 g.), oil.

後処理

  1. extractionthe solution was extracted with methylene chloride three times
  2. washThe extract was washed with water
  3. dry with materialan aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in turn, and dried over magnesium sulfate
  4. concentrationThe solution was concentrated in vacuo

出典と根拠

ORDレコード
ord-60ef2266988f4338aa908f4602222e91
出典データセット
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04447430

反応ノート

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