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Hydrochloric Acid → 2-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole

HRID 1534767
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HRID 1534767 반응식
[OH-].[K+].[CH2:3]([C:9]1[S:10][C:11]([C:14]2[CH:23]=[CH:22][C:21]3[C:16](=[CH:17][CH:18]=[C:19]([O:24]C(=O)C)[CH:20]=3)[CH:15]=2)=[N:12][N:13]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].O.Cl>C(O)C>[CH2:3]([C:9]1[S:10][C:11]([C:14]2[CH:23]=[CH:22][C:21]3[C:16](=[CH:17][CH:18]=[C:19]([OH:24])[CH:20]=3)[CH:15]=2)=[N:12][N:13]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 14797Potassium HydroxideHCID 199079422-Hexyl-5-(6-acetoxynaphthalene-2-yl)-1,3,4-thiadiazole

생성물 1

HCID 1360772002-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole수율 74.3%

시약·촉매·용매 1

HCID 702
Ethanol
용매

실험 절차

1.50 g (22.7 mM) of potassium hydroxide was dissolved in 72 ml of ethanol at 60°-65° C. To the solution, 2.90 g (8.18 mM) of 2-hexyl-5-(6-acetoxynaphthalene-2-yl)-1,3,4-thiadiazole was added, followed by stirring for 20 minutes at 60°-65° C. The reaction mixture was poured into 200 ml of iced water and 3 ml of concentrated hydrochloric acid was added thereto to precipitate a crystal. The crystal was recovered by filtration and washed with water to obtain 1.90 g of 2-hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole (Yield: 71.9 %). ##STR138##

후처리

  1. additionwas added
  2. customto precipitate a crystal
  3. filtrationThe crystal was recovered by filtration
  4. washwashed with water

출처 및 근거

ORD 기록
ord-024ae5efd6834466b85091b87e28a033
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05091109

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