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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → (6-Methylpyridin-3-yl)acetic acid

HRID 2369259
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HRID 2369259 반응식
[CH3:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9](N2CCOCC2)=S)=[CH:4][CH:3]=1.[OH-:17].[Na+].[OH2:19].CCO>>[CH3:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9]([OH:19])=[O:17])=[CH:4][CH:3]=1
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참가 물질

4

반응물 3

HCID 14798Sodium HydroxideHCID 2727779HCID 2727779, 화합물HCID 19096565Water ethanol

생성물 1

HCID 22507698(6-Methylpyridin-3-yl)acetic acid

실험 절차

Crude 2-(6-Methyl-pyridin-3-yl)-1-morpholin-4-yl-ethanethione (39.5 mmol, 9.685 g) was suspended in 2:1 H2O/EtOH (75 cm3). NaOH (3.3 eq., 118.5 mmol, 4.8 g) added and the reaction heated to reflux for 16 hours. Volatiles were then removed from the cooled reaction medium, and the aqueous residue extracted with DCM (3×50 cm3). The pH was adjusted to precisely pH 7.0 with HCl, and a further DCM extraction performed (3×50 cm3). Water was removed from the residue, and the obtained solids slurried in methanol, filtered, and the filtrate evaporated to dryness. The orange solid obtained gave spectroscopic data consistent with the desired product. Mass recovery is typically >100% however this is due to NaCl within the product.

후처리

  1. temperaturethe reaction heated
  2. temperatureto reflux for 16 hours
  3. customVolatiles were then removed from the cooled reaction medium
  4. extractionthe aqueous residue extracted with DCM (3×50 cm3)
  5. extractiona further DCM extraction
  6. customWater was removed from the residue
  7. filtrationfiltered
  8. customthe filtrate evaporated to dryness
  9. customThe orange solid obtained

출처 및 근거

ORD 기록
ord-c837319fb1694b448e9e86475f532451
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703952B2

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