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Dimethylamine → 4-[2-(Dimethylamino)-2-oxoethyl]benzeneacetic acid

HRID 1722420
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HRID 1722420 반응식
[C:1]1([CH2:11][C:12]([OH:14])=O)[CH:6]=[CH:5][C:4]([CH2:7][C:8]([OH:10])=[O:9])=[CH:3][CH:2]=1.[CH3:15][NH:16][CH3:17]>CN(C)C=O.C([O-])([O-])=O.[K+].[K+]>[CH3:15][N:16]([CH3:17])[C:12](=[O:14])[CH2:11][C:1]1[CH:6]=[CH:5][C:4]([CH2:7][C:8]([OH:10])=[O:9])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 674DimethylamineHCID 81760p-Phenylenediacetic acid

생성물 1

HCID 141809534-[2-(Dimethylamino)-2-oxoethyl]benzeneacetic acid수율 8.5%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 11430Potassium Carbonate용매

실험 절차

N,N'-Carbonyldiimidazole (11.4 g) was added to a stirred solution of 1,4-phenylenediacetic acid (11.4 g) in dry dimethylformamide (300 ml) under an atmosphere of nitrogen. The mixture was stirred at 20° for 2 h as dimethylamine gas (about 10 g) was bubbled through. The reaction mixture was then stirred at 20° for 3 h and evaporated in vacuo to leave a brown oil which was diluted with saturated K2CO3 solution (50 ml). The resulting mixture was evaporated in vacuo to leave an off-white solid which was triturated with EA (2×200 ml). The organic phase was discarded and the aqueous phase was acidified (pH1) with 5M hydrochloric acid to precipitate an off-white solid which was triturated with absolute ethanol (25 ml) and filtered to give the title compound (1.1 g) as a fine white solid m.p. 163°-165° (softening at 160°).

후처리

  1. customwas bubbled through
  2. customevaporated in vacuo
  3. customto leave a brown oil which
  4. customThe resulting mixture was evaporated in vacuo
  5. customto leave an off-white solid which
  6. customwas triturated with EA (2×200 ml)
  7. customto precipitate an off-white solid which
  8. customwas triturated with absolute ethanol (25 ml)
  9. filtrationfiltered

출처 및 근거

ORD 기록
ord-27ca6a46d4c9461ca6f31d13f0c46ac9
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04855314

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