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Hydrochloric Acid → HCID 28401656、化合物

HRID 238331
ノート
印刷プレビュー

反応式

HRID 238331 の反応式
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([NH:9]C(=O)C)[CH:8]=1.[OH-].[Na+]>C(O)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([CH:8]=1)[NH2:9]
参加物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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 66917186HCID 66917186、化合物

生成物 1

HCID 28401656HCID 28401656、化合物収率 101.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Concentrated hydrochloric acid (5.8 ml) was added to an ethanol solution (100 ml) of N-(5-bromo-2-cyclopentyloxyphenyl)acetamide (3.4 g, 11.4 mmol), and the resulting mixture was stirred for 3 hours while heating under reflux. After the reaction mixture was cooled to room temperature, a 5N sodium hydroxide solution (14.2 ml) was added to obtain a pH of 11. The resulting mixture was then extracted with dichloromethane. The organic layer was washed with a saturated sodium chloride aqueous solution, and then concentrated under reduced pressure. The residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1). The purified product was concentrated under reduced pressure to thereby obtain 2.97 g of oily pale yellow 5-bromo-2-cyclopentyloxyaniline (yield: 100%).

後処理

  1. temperaturewhile heating
  2. temperatureunder reflux
  3. customto obtain a pH of 11
  4. extractionThe resulting mixture was then extracted with dichloromethane
  5. washThe organic layer was washed with a saturated sodium chloride aqueous solution
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1)
  8. concentrationThe purified product was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-113948156d4c41c281f290411a4d994c
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08642619B2

反応ノート

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