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Hydrochloric Acid → Methyl 3-{[2-(dimethylamino)-2-oxoethyl]oxy}benzoate

HRID 1892899
ノート
印刷プレビュー

反応式

HRID 1892899 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].C([O-])([O-])=O.[K+].[K+].Cl[CH2:19][C:20]([N:22]([CH3:24])[CH3:23])=[O:21].Cl>CN(C=O)C>[CH3:23][N:22]([CH3:24])[C:20](=[O:21])[CH2:19][O:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]
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 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 758862-chloro-N,N-dimethylacetamideHCID 88068Methyl 3-Hydroxybenzoate

生成物 1

HCID 58054508Methyl 3-{[2-(dimethylamino)-2-oxoethyl]oxy}benzoate収率 94%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

A mixture of methyl 3-hydroxybenzoate (Aldrich) (1.52 g, 10 mmol) and K2CO3 (1.38 g, 10 mmol) in DMF (10 mL) was stirred for 1 h. 2-Chloro-N,N-dimethylacetamide (Merck) (1.03 mL, 10 mmol) was added and the mixture was stirred for 1 h at RT and then stood at RT for 6 days. The mixture was then acidified with 2M HCl and extracted with EtOAc. The aqueous layer was extracted twice more with EtOAc and the combined organic solutions were washed with 2M HCl (×3), aq. sat NaHCO3, brine, dried (MgSO4) and evaporated under reduced pressure to give the title compound (2.22 g, 94%) as a white solid. LCMS (System A) RT=0.80 min, 91%, ES+ve m/z 238 (M+H)+.

後処理

  1. stirringthe mixture was stirred for 1 h at RT
  2. waitstood at RT for 6 days
  3. extractionextracted with EtOAc
  4. extractionThe aqueous layer was extracted twice more with EtOAc
  5. washthe combined organic solutions were washed with 2M HCl (×3)
  6. dry with materialdried (MgSO4)
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-02cbb447673f4761b0674c7c2f9a7cae
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507543B2

反応ノート

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