Cerium(III) chloride → HCID 54572386、化合物

HRID 1731651ノート

反応式

HRID 1731651 の反応式
[O:1]=[C:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:4]=[CH:3]1.[Cl-].[Ce+3].[Cl-].[Cl-].[BH4-].[Na+]>CO>[OH:1][CH:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:4]=[CH:3]1

参加物

5

反応物 3

HCID 24636Cerium(III) chlorideHCID 4311764Sodium borohydrideHCID 14430179HCID 14430179、化合物

生成物 1

HCID 54572386HCID 54572386、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a mixture of 0.36 g of methyl 4-oxocyclohex-2-enepropionate and 500 ml of 0.4M cerium chloride in methanol there was added carefully 0.07 g of sodium borohydride and the mixture was stirred for 10 minutes at room temperature. The reaction was quenched with 2 ml of water and the methanol solvent was removed under reduced pressure. The residue was partitioned between 10 ml of water and 50 ml of ether and the separated organic layer was dried over magnesium sulfate. Evaporation of the solvent from the organic solution gave methyl 4-hydroxycyclohex-2-enepropionate as a clear oil which was used without further purification. 1H NMR (CDCl3) δ 3.56 (s, 3H); 3.90-4.30 (m, 1H); 5.50-5.75 (m, 2H).

後処理

  1. customThe reaction was quenched with 2 ml of water
  2. customthe methanol solvent was removed under reduced pressure
  3. customThe residue was partitioned between 10 ml of water and 50 ml of ether
  4. dry with materialthe separated organic layer was dried over magnesium sulfate
  5. customEvaporation of the solvent from the organic solution

出典と根拠

ORDレコード
ord-18b35497b407447c86fa0e9444abbf6c
出典データセット
uspto-grants-1986_11
特許番号
US04622422

反応ノート

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