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Glycine → HCID 89815163, 화합물

HRID 1481191
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HRID 1481191 반응식
[C:1]1([CH3:20])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[O:7][C:8]1[CH:9]=[C:10]([C:17]([OH:19])=O)[C:11](=[CH:15][CH:16]=1)[C:12]([OH:14])=O.[NH2:21][CH2:22][C:23]([OH:25])=[O:24]>>[O:14]=[C:12]1[C:11]2[C:10](=[CH:9][C:8]([O:7][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=3[CH3:20])=[CH:16][CH:15]=2)[C:17](=[O:19])[N:21]1[CH2:22][C:23]([OH:25])=[O:24]
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참가 물질

3

반응물 2

HCID 750GlycineHCID 17846261HCID 17846261, 화합물

생성물 1

HCID 89815163HCID 89815163, 화합물

반응 조건

온도
230 °C

실험 절차

A mixture of 4-(o-tolyloxy)phthalic acid (9.5 g, 35.0 mmol) and glycine (2.6 g, 35.0 mmol) was ground thoroughly in a mortar. The powder was then transferred to a flask and heated to 220-240° C. under high vacuum for 30 minutes. The reaction crude was cooled to room temperature to give the title compound in 10.2 g. 1H NMR (DMSO, 200 MHz): δ=7.89 (d, 1H, J=8.0 Hz), 7.42-7.08 (m, 6H), 4.27 (s, 2H), 2.14 (s, 3H).

후처리

  1. customThe powder was then transferred to a flask
  2. customThe reaction crude
  3. temperaturewas cooled to room temperature

출처 및 근거

ORD 기록
ord-ff134a0526a54dfa82f3150fc293941d
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409892B2

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