17372-87-1 → 2-Mercapto-4-Methylpentanoic Acid

HRID 1249343

반응식

HRID 1249343 반응식
[OH-].[Na+].C1C=[C:7]([C:9]2[C:23]3C(=C(Br)C([O-])=C(Br)C=3)OC3[C:10]=2C=C(Br)C(C=3Br)=O)[C:6]([C:29]([O-:31])=[O:30])=CC=1.[Na+].[Na+].C(=[S:37])([O-])[O-].[Na+].[Na+]>O>[SH:37][CH:6]([CH2:7][CH:9]([CH3:23])[CH3:10])[C:29]([OH:31])=[O:30]

참가 물질

5

반응물 3

HCID 1104817372-87-1HCID 14798Sodium HydroxideHCID 20782767HCID 20782767, 화합물

생성물 1

HCID 136332582-Mercapto-4-Methylpentanoic Acid수율 34%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A total of 1.25 g. (6.5 mmoles) of the product prepared above is taken up in 2 ml. of water. Sufficient 1 N sodium hydroxide is added to dissolve the bromo acid. To this mixture, there is added 5 ml. of 40% sodium thiocarbonate and the vessel is closed and allowed to stand at room temperature for 24 hours. At the end of this period, the solution is acidified with 18 N. sulfuric acid, and extracted with 2 10 ml. portions of ethyl ether. The combined extracts are dried over anhydrous magnesium sulfate and filtered. The filtrate is concentrated to approximately half its volume and chromatographed on a silica gel column (2.2×30 cm). The original solution is eluted with 150 ml. of ethyl ether, and the product recovered by evaporation of the solvent in the eluate. The yield is approximately 34%. The Rf values (TLC) are 0.88 and 1.0 on silica gel and cellulose plates (n-butanol/acetic acid/water-12/3/5).

후처리

  1. additionTo this mixture, there is added 5 ml
  2. extractionsulfuric acid, and extracted with 2 10 ml
  3. dry with materialThe combined extracts are dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate is concentrated to approximately half its volume
  6. customchromatographed on a silica gel column (2.2×30 cm)
  7. washThe original solution is eluted with 150 ml
  8. customof ethyl ether, and the product recovered by evaporation of the solvent in the eluate

출처 및 근거

ORD 기록
ord-52e99b5cc837459a82e01b3c0512afe2
출처 데이터셋
uspto-grants-1986_12
특허 번호
US04631270

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