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Thionyl Chloride → HCID 21443926, 화합물

HRID 328110
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HRID 328110 반응식
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([OH:13])=O)=[CH:6][CH:5]=1)(=[NH:3])[NH2:2].S(Cl)([Cl:16])=O>C1C=CC=CC=1.CN(C)C=O>[ClH:16].[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([Cl:16])=[O:13])=[CH:6][CH:5]=1)(=[NH:3])[NH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 103133572-(4-carbamimidoylphenyl)acetic Acid

생성물 1

HCID 21443926HCID 21443926, 화합물수율 98.6%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 241Benzene용매

실험 절차

5.35 g of 4-amidinophenylacetic acid (M.p. 295° to 297° C, decomposition) were suspended in 45 ml of anhydrous benzene. Two drops of dimethylformamide and 17.9 g of thionyl chloride were added and the whole was heated for 11/2 hours under reflux. After cooling, the solid product was filtered off with suction, washed with anhydrous benzene and dried under reduced pressure. 6.9 g of 4-amidino-phenylacetyl chloride-hydrochloride melting at 174° to 177° C (decomposition) were obtained.

후처리

  1. temperaturethe whole was heated for 11/2 hours
  2. temperatureunder reflux
  3. temperatureAfter cooling
  4. filtrationthe solid product was filtered off with suction
  5. washwashed with anhydrous benzene
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-d93d65c20ae7453291def8277cf8f509
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04016159

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