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Hydrochloric Acid → Methyl 4-(1-aminocyclopropyl)benzoate

HRID 72393
ノート
印刷プレビュー

反応式

HRID 72393 の反応式
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][CH:4]=1)#[N:2].[CH2:13]([Mg]Br)[CH3:14].B(F)(F)F.CCOCC.Cl>C(OCC)C.[Ti+4]>[NH2:2][C:1]1([C:3]2[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][CH:4]=2)[CH2:14][CH2:13]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 8000Boron trifluoride etherateHCID 70791Methyl 4-cyanobenzoateHCID 178418443HCID 178418443、化合物

生成物 1

HCID 45140209Methyl 4-(1-aminocyclopropyl)benzoate

試薬・触媒・溶媒 2

HCID 114942Titanium cation (4+)触媒
HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

To the solution of methyl 4-cyanobenzoate (100 g, 620 mmol) in diethyl ether (3 L) was added titanium (IV) isospropoxide (194 g, 682 mmol), followed by dropwise addition of ethylmagnesium bromide 3M solution in diethylether (450 ml, 1.36 mol) at −70° C. The mixture was stirred for 1 h, and then boron trifluoride etherate (157 ml, 1.24 mol) was added at once. After 2 hours, aqueous HCl (5%) was added until the pH showed acidy, then the mixture was filtered. The solid was washed with ethylacetate. The aqueous phase was separated and the organic layer was washed with water. All aqueous layers were collected together, basified with 1M NaOH and extracted with ethylacetate. The organic layer was dried (Na2SO4) and concentrated to afford the title compound (D6) (32.0 g).

後処理

  1. waitAfter 2 hours
  2. filtrationthe mixture was filtered
  3. washThe solid was washed with ethylacetate
  4. customThe aqueous phase was separated
  5. washthe organic layer was washed with water
  6. customAll aqueous layers were collected together
  7. extractionextracted with ethylacetate
  8. dry with materialThe organic layer was dried (Na2SO4)
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-69fbaee20a4b43819e198be7fc984b6b
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08828987B2

反応ノート

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