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Ethanol → 2-p-tolylbenzo[d]oxazole-5-carboxylic acid

HRID 426452
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반응식

HRID 426452 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][C:14]([C:17]([O:19]C)=[O:18])=[CH:13][C:11]=3[N:12]=2)=[CH:4][CH:3]=1.[OH-].[Na+].C(O)C>O>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][C:14]([C:17]([OH:19])=[O:18])=[CH:13][C:11]=3[N:12]=2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 20390926HCID 20390926, 화합물

생성물 1

HCID 115578892-p-tolylbenzo[d]oxazole-5-carboxylic acid

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A solution contaning 16.0 g. (0.06 mole) of methyl 2-(4-methylphenyl)-5-benzoxazolecarboxylate (1a), 4.0 g. (0.1 mole) of sodium hydroxide, and 50 ml. of water in 275 ml. of ethanol was stirred at 25° for 16 hours. The reaction mixture was poured into 1 l. of water. Acidification gave a white precipitate which was filtered, washed with water, and when air-dried amounted to 14.44 g. (95%) of 2-(4-methylphenyl)-5-benzoxazolecarboxylic acid (1b). The ir and nmr spectra were consistent with the proposed structure.

후처리

  1. additionThe reaction mixture was poured into 1 l
  2. customAcidification gave a white precipitate which
  3. filtrationwas filtered
  4. washwashed with water, and when
  5. customair-dried

출처 및 근거

ORD 기록
ord-7ddf6379cf544c1286f7d4579958906a
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04169837

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