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Hydrochloric Acid → 2-Chloro-6-sulfanylbenzoic acid

HRID 1885978
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HRID 1885978 반응식
[Cl:1][C:2]1[C:7]([C:8]([OH:10])=[O:9])=[C:6]([S:11]C(OCC)=S)[CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].Cl>CO>[Cl:1][C:2]1[C:7]([C:8]([OH:10])=[O:9])=[C:6]([SH:11])[CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 19876591HCID 19876591, 화합물

생성물 1

HCID 144382762-Chloro-6-sulfanylbenzoic acid수율 106%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a stirred solution of 2.0 grams (0.007 mole) of 6-chloro-2-[ethoxy(thiocarbonyl)thio]benzoic acid in 50 mL of methanol was added 30 ml of aqueous 10% sodium hydroxide. The reaction mixture was warmed to reflux where it stirred for about 18 hours. After this time the reaction mixture was cooled to ambient temperature and was acidified with concentrated hydrochloric acid. The mixture was extracted with ethyl acetate, and the extract was dried with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure to yield 1.4 grams of 6-chloro-2-mercaptobenzoic acid. The nmr spectrum was consistent with the proposed structure.

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후처리

  1. temperatureThe reaction mixture was warmed
  2. temperatureto reflux where it
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialthe extract was dried with magnesium sulfate
  5. filtrationThe mixture was filtered
  6. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-75137d211a5a4be38a1cac1b8a758ae9
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05149357

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