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Hydrochloric Acid → HCID 54071646, 화합물

HRID 1659867
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반응식

HRID 1659867 반응식
[CH3:1][C:2]1[S:3][C:4]([CH:7]=[CH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][CH2:16][CH:17]2[O:19][CH2:18]2)=[N:5][N:6]=1.[ClH:20]>C(O)C.CCOCC>[CH3:1][C:2]1[S:3][C:4]([CH:7]=[CH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][CH2:16][CH:17]([OH:19])[CH2:18][Cl:20])=[N:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 53934759HCID 53934759, 화합물

생성물 1

HCID 54071646HCID 54071646, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 3283Diethyl Ether용매

실험 절차

1 g of 2-methyl-5-[2-(2,3-epoxypropoxy)-styryl]-1,3,4-thiadiazole is left to stand for 12 hours in a mixture of 100 ml of ethanol and 5 ml of a 3 N solution of hydrogen chloride in ether. The precipitate formed is filtered off, washed neutral with ether and chromatographed on silica gel, using chloroform. The product eluates, when evaporated to dryness, give spectroscopically pure 2-methyl-5-[2-(2-hydroxy-3-chloro-propoxy)-styryl]-1,3,4-thiadiazole of melting point 168°-170° C.

후처리

  1. customThe precipitate formed
  2. filtrationis filtered off
  3. washwashed neutral with ether
  4. customchromatographed on silica gel
  5. customwhen evaporated to dryness

출처 및 근거

ORD 기록
ord-f98267158719489c8a7f9b4f3ec190a7
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04305950

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