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2-Naphthol → 3-Hydroxy-2-naphthoic acid

HRID 259477
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인쇄 미리보기

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HRID 259477 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[OH:11].[OH-:12].[Na+].C1(OCC[O:27][C:28]2C3C(=CC=CC=3)C=CC=2)C2C(=CC=CC=2)C=CC=1>>[OH:11][C:2]1[C:3]([C:28]([OH:27])=[O:12])=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 86632-NaphtholHCID 14798Sodium HydroxideHCID 2356171-[2-(1-naphthyloxy)ethoxy]naphthalene

생성물 1

HCID 71043-Hydroxy-2-naphthoic acid수율 72%

반응 조건

온도
260 °C

실험 절차

A stirred autoclave is charged with 1210 parts of β-naphthol, 620 parts of caustic soda solution (50% by weight strength) and 300 parts of 1,2-dinaphthoxyethane. As described in Example 4 the mixture is heated to an internal temperature of 260° C. while stirring and kept at this temperature for ten minutes. During this period the residual moisture is removed from the autoclave by applying 100 mm pressure. Dehydration is practically complete. Carbon dioxide is then introduced at the internal temperature of 260° C. up to a pressure of 7 atmospheres. After the absorption of carbon dioxide is completed the β-naphthol formed in the reaction is distilled off in vacuo. Further processing is carried out as in Example 5. 525 parts (72% of theory based on reacted β-naphthol) of 2-hydroxy-naphthalene-3-carboxylic acid is obtained with a melting point of 212° to 215° C.

후처리

  1. waitkept at this temperature for ten minutes
  2. customDuring this period the residual moisture is removed from the autoclave
  3. additionCarbon dioxide is then introduced at the internal temperature of 260° C. up to a pressure of 7 atmospheres
  4. customAfter the absorption of carbon dioxide
  5. customformed in the reaction
  6. distillationis distilled off in vacuo

출처 및 근거

ORD 기록
ord-90c0baec0c8d4bcb9c27cf4e7948dc9a
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04038309

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