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Hydrochloric Acid → 3-(Methylthio)-5-(trifluoromethyl)benzoic acid

HRID 1606759
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HRID 1606759 반응식
[SH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1)[C:5]([OH:7])=[O:6].[OH-].[Na+].[CH3:17]I.Cl>C(O)C>[CH3:17][S:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:10]=1)[C:5]([OH:7])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 21542284HCID 21542284, 화합물

생성물 1

HCID 214459703-(Methylthio)-5-(trifluoromethyl)benzoic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 10 g. (0.045 mole) of 3-mercapto-5-trifluoromethylbenzoic acid, and 100 ml. of 1N sodium hydroxide in 100 ml. of ethanol is added 3.8 ml. (0.06 mole) of methyl iodide. After the reaction has stirred at room temperature for one hour, it is acidified with 12N hydrochloric acid, and the precipitate of the final product is filtered and dried,8.6 g., m.p. 135°-140° C. A sample is sublimed at 175° C. and 0.03 mm pressure, m.p. 151°-152.5° C.

후처리

  1. filtrationthe precipitate of the final product is filtered
  2. customdried
  3. customis sublimed at 175° C.

출처 및 근거

ORD 기록
ord-6ccdc6fdae374e30a10ed670f7e67ae9
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03953595

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