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Ammonium Chloride → HCID 66803969、化合物

HRID 2190988
ノート
印刷プレビュー

反応式

HRID 2190988 の反応式
[CH3:1][C:2]1[CH2:3][CH:4]2[CH:7]([CH:8]=1)[C:6]([CH2:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])([CH2:9][N+:10]([O-])=O)[CH2:5]2.[Cl-].[NH4+]>C(O)C.O.[Fe]>[NH2:10][CH2:9][C:6]1([CH2:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:5][CH:4]2[CH:7]1[CH:8]=[C:2]([CH3:1])[CH2:3]2
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 25517Ammonium ChlorideHCID 66803697HCID 66803697、化合物

生成物 1

HCID 66803969HCID 66803969、化合物収率 28%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

Tert-butyl [3-methyl-6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate (1.12 g, 3.99 mmol) was dissolved in ethanol (20 mL) and water (10 mL). To the solution, iron powder (892.8 mg, 15.9 mmol) and ammonium chloride (211.5 mg, 3.99 mmol) were added, and the mixture was stirred for 4 hours under heating to reflux. The mixture was allowed to cool, then diluted with saturated saline, a saturated aqueous solution of sodium bicarbonate, and ethyl acetate, and filtered through Celite to remove insoluble matter. The filtrate was separated into organic and aqueous layers. The organic layer was washed with saturated saline, then dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. To the residue, a 4 N solution of hydrochloric acid in ethyl acetate (5 mL) was added, and the mixture was stirred at room temperature for 1 hour. Then, the solvent was distilled off under reduced pressure. The residue was suspended in dichloromethane. To the suspension, triethylamine was added dropwise, and the resulting powder was collected by filtration, then washed with dichloromethane, and then dried to obtain the compound of interest as a white powder (105.8 mg, 28%).

後処理

  1. temperatureunder heating to reflux
  2. temperatureto cool
  3. additiondiluted with saturated saline
  4. filtrationa saturated aqueous solution of sodium bicarbonate, and ethyl acetate, and filtered through Celite
  5. customto remove insoluble matter
  6. customThe filtrate was separated into organic and aqueous layers
  7. washThe organic layer was washed with saturated saline
  8. dry with materialdried over anhydrous magnesium sulfate
  9. distillationthe solvent was then distilled off under reduced pressure
  10. additionTo the residue, a 4 N solution of hydrochloric acid in ethyl acetate (5 mL) was added
  11. stirringthe mixture was stirred at room temperature for 1 hour
  12. distillationThen, the solvent was distilled off under reduced pressure
  13. additionTo the suspension, triethylamine was added dropwise
  14. filtrationthe resulting powder was collected by filtration
  15. washwashed with dichloromethane
  16. customdried

出典と根拠

ORDレコード
ord-6213d0f20d204bb2b2734e185db5d49f
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324425B2

反応ノート

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