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Sulfuric Acid → Propanoic acid, 2-chloro, 3-butenyl ester

HRID 6573
ノート
印刷プレビュー

反応式

HRID 6573 の反応式
[CH3:1][CH:2]([C:4]([OH:6])=[O:5])[Cl:3].[CH2:7]=[CH:8][CH2:9][CH2:10]O.S(=O)(=O)(O)O.C(=O)([O-])[O-].[Na+].[Na+]>C(OC)(C)(C)C.O>[CH3:1][CH:2]([C:4]([O:6][CH2:10][CH2:9][CH:8]=[CH2:7])=[O:5])[Cl:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 1118Sulfuric AcidHCID 10340Sodium CarbonateHCID 117342-Chloropropionic acidHCID 693893-Buten-1-ol

生成物 1

HCID 523724Propanoic acid, 2-chloro, 3-butenyl ester

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 15413

実験手順

CH3CHClCOOH (50 g) and CH2═CHCH2CH2OH (75 ml) were put into a flask, and 10 ml of concentrated sulfuric acid was added dropwise, followed by stirring at room temperature for 10 minutes. The reaction solution was poured into 250 ml of a saturated sodium carbonate aqueous solution. 150 ml of water and 150 ml of t-butylmethyl ether were added for liquid separation to obtain a t-butylmethyl ether layer as an organic layer. The organic layer was washed with 150 ml of water, dried over magnesium sulfate and then subjected to filtration to obtain a crude liquid. The crude liquid was concentrated to obtain CH3CHClCOOCH2CH2CH═CH2.

後処理

  1. washThe organic layer was washed with 150 ml of water
  2. dry with materialdried over magnesium sulfate
  3. filtrationsubjected to filtration
  4. customto obtain a crude liquid
  5. concentrationThe crude liquid was concentrated

出典と根拠

ORDレコード
ord-da416716b18045318a79e460f3c3b0be
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07083705B2

反応ノート

読み込み中…

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