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Iodine → ethyl 6-oxodecanoate

HRID 851836
ノート
印刷プレビュー

反応式

HRID 851836 の反応式
[CH2:1](I)[CH2:2][CH2:3][CH3:4].II.[Cl-].[CH2:9]([O:11][C:12](=[O:20])[CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=O)[CH3:10].S(=O)(=O)(O)O>[Cu].[Zn].O.C1(C)C=CC=CC=1.C(OCCCC)(=O)C>[O:19]=[C:17]([CH2:1][CH2:2][CH2:3][CH3:4])[CH2:16][CH2:15][CH2:14][CH2:13][C:12]([O:11][CH2:9][CH3:10])=[O:20]
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

9

反応物 4

HCID 807IodineHCID 1118Sulfuric AcidHCID 10962Butyl iodideHCID 86624202Adipic acid monoethyl ester chloride

生成物 1

HCID 11063798ethyl 6-oxodecanoate

試薬・触媒・溶媒 4

HCID 10290809Zinc copper couple触媒
HCID 962
Water
溶媒
HCID 1140Toluene溶媒
HCID 31272Butyl Acetate溶媒

反応条件

温度
115 °C

実験手順

A mixture of activated zinc-copper catalyst (11.5 g), butyl acetate (4 g), toluene (5 g), butyl iodide (15 g) and iodine (3 mg) was heated at 110-120° C. for 2 hours. The mixture was then added dropwise with adipic acid monoethyl ester chloride(15.7 g) at 0° C., and then was allowed to react. After the reaction was completed, ice-cooled water was added to the reaction solution, and then decomposed with dilute sulfuric acid. The oily layer was extracted with ether, washed with aqueous sodium hydrogencarbonate, washed with water, and then dried. The residue was evaporated to remove the solvent, and then distilled, thereby giving ethyl 6-oxodecanoate (8.1 g).

後処理

  1. customto react
  2. additionwas added to the reaction solution
  3. extractionThe oily layer was extracted with ether
  4. washwashed with aqueous sodium hydrogencarbonate
  5. washwashed with water
  6. customdried
  7. customThe residue was evaporated
  8. customto remove the solvent
  9. distillationdistilled

出典と根拠

ORDレコード
ord-f8e59d31c55344dab18d4c459cf6a61a
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07252849B2

反応ノート

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