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Pyridine → Trimethylsilyl crotonate

HRID 714581
ノート
印刷プレビュー

反応式

HRID 714581 の反応式
[C:1]([OH:6])(=[O:5])/[CH:2]=[CH:3]/[CH3:4].[CH3:7][Si:8]([CH3:11])([CH3:10])Cl.N1C=CC=CC=1>C(OCC)C>[C:1]([O:6][Si:8]([CH3:11])([CH3:10])[CH3:7])(=[O:5])/[CH:2]=[CH:3]/[CH3:4]
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 1049PyridineHCID 6397ChlorotrimethylsilaneHCID 637090Crotonic Acid

生成物 1

HCID 5702560Trimethylsilyl crotonate収率 62%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
38 °C

実験手順

To a single-neck reaction flask (250 mL) were added of crotonic acid (10.750 g, 0.125 mol), anhydrous ethyl ether (125 mL) and trimethyl chlorosilane (19 mL, 0.150 mol). The mixture was stirred for 5 min. Pyridine (12 mL, 0.150 mol) was dropwise added into the resulting mixture under stirring at the temperature of 35° C. After the addition finished, the mixture was warmed up to the temperature of 38° C. and stirred under relux for 3 hr. The white solid was filtered in vacuo. Ethyl ether was evaporated under atmospheric pressure. The resultant was distilled under reduced pressure to collect the fraction under 10 mmHg at the temperature of 46° C.-48° C. to give (E)-trimethylsilyl 2-butenoate as a colorless liquid (12.242 g). Yield: 62.0%.

後処理

  1. stirringunder stirring at the temperature of 35° C
  2. additionAfter the addition
  3. stirringstirred under relux for 3 hr
  4. filtrationThe white solid was filtered in vacuo
  5. customEthyl ether was evaporated under atmospheric pressure
  6. distillationThe resultant was distilled under reduced pressure
  7. customto collect the fraction under 10 mmHg at the temperature of 46° C.-48° C.

出典と根拠

ORDレコード
ord-d93b544677664a049491f249d7e69701
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187458B2

反応ノート

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