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Ozone → HCID 54077346、化合物

HRID 1417761
ノート
印刷プレビュー

反応式

HRID 1417761 の反応式
[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9])[CH:2]=C.[O:14]=[O+][O-]>C(Cl)Cl>[O:14]=[CH:2][CH2:1][O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24823OzoneHCID 64838843-(Allyloxy)Benzoic Acid

生成物 1

HCID 54077346HCID 54077346、化合物収率 93%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 300 mg (1.68 mmol) of 3-(2-propenyloxy)benzoic acid in 5 mL of methylene chloride is cooled to -78° C. Ozone is introduced by bubbling the gas into the solution through a glass tube until a blue color persists. The solution is then purged with a stream of argon and 1 mL of methyl sulfide is added. The solution is diluted with 20 mL of ether and washed with water. The organic layer is separated and allowed to stand over magnesium sulfate then concentrated in vacuo to give 283 mg (93%) of 3-(2-oxoethoxy)benzoic acid as a colorless oil. The product is utilized in the next reaction without further purification: m.p. 120°-130°; the 1H NMR (300 MHz, CDCl3) is consistent with the desired product; IR (KBr) 3400, 3000, 1680, 1590 cm-1 ; MS (CI low res) m/e 181 (M+H), 163, 139, 119.

後処理

  1. customby bubbling the gas into the solution through a glass tube until a blue color persists
  2. customThe solution is then purged with a stream of argon and 1 mL of methyl sulfide
  3. additionis added
  4. additionThe solution is diluted with 20 mL of ether
  5. washwashed with water
  6. customThe organic layer is separated
  7. concentrationthen concentrated in vacuo

出典と根拠

ORDレコード
ord-af5bdeea55754aa6bfeffade1e978fc8
出典データセット
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05877296

反応ノート

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