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Ethanol → HCID 13013932, 화합물

HRID 444149
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HRID 444149 반응식
[CH:1]1[C:6]2[CH2:7][NH:8][C:9]3[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=3[S:11](=[O:13])(=[O:12])[C:5]=2[CH:4]=[C:3]([C:18]([O:20]C)=[O:19])[CH:2]=1.[OH-].[K+].O.C(O)C>O1CCOCC1>[CH:1]1[C:6]2[CH2:7][NH:8][C:9]3[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=3[S:11](=[O:13])(=[O:12])[C:5]=2[CH:4]=[C:3]([C:18]([OH:20])=[O:19])[CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 962WaterHCID 14797Potassium HydroxideHCID 13013933Methyl 10,11-dihydrodibenzo[b,f][1,4]thiazepin-3-carboxylate 5,5-Dioxide

생성물 1

HCID 13013932HCID 13013932, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Stir a mixture of 3.03 gm. (10 mmole) of the ester of Example 15, 2.24 gm. (20 mmole) of 85% aqueous potassium hydroxide, 11 ml. of water, 55 ml. of ethanol and 5.5 ml. of dioxane under nitrogen for 2 hours. Concentrate the reaction mixture to the point of crystallization and dilute with 40 ml. of water. Filter and acidify with acetic acid. Separate the precipitate by filtration and wash with water and dry to obtain the title product (m.p. 304°-306° C.).

후처리

  1. additiona mixture of 3.03 gm
  2. concentrationConcentrate the reaction mixture
  3. customto the point of crystallization
  4. additiondilute with 40 ml
  5. filtrationFilter
  6. customSeparate the precipitate
  7. filtrationby filtration
  8. washwash with water
  9. customdry

출처 및 근거

ORD 기록
ord-20952a204f2a4749b2c12d833414a7ee
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263207

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