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Hydrochloric Acid → HCID 67408131, 화합물

HRID 1913414
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HRID 1913414 반응식
C([O:5][C:6](=[O:18])[CH:7](C#N)[C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH3:15])=[CH:10][N:9]=1)(C)(C)C.Cl>O>[CH2:14]([C:11]1[CH:12]=[CH:13][C:8]([CH2:7][C:6]([OH:18])=[O:5])=[N:9][CH:10]=1)[CH3:15]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 67408263HCID 67408263, 화합물

생성물 1

HCID 67408131HCID 67408131, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
104 °C

실험 절차

Cyano-(5-ethyl-pyridin-2-yl)-acetic acid tert-butyl ester (7.3 g) was mixed with 70 mL of water and 70 mL of 12N HCl and was heated at 104° C. for 3 hours before removing the volatiles in vacuo. Water was added to dissolve the solids and the pH of the solution was adjusted to 9-10 with 2N NaOH. The solution was washed with 2-methylTHF (2×). The aqueous solution was adjusted to pH 4 with 2N HCl and was concentrated under vacuum to an oily solid. The residue was triturated with hot chloroform and heptanes to afford (5-ethylpyridin-2-yl)acetic acid (SM-1ac) as a tan solid (3.88 g, 31%, 3 steps). MS (ES+) 166.1 (M+H)+. 1H NMR (DMSO-d6) δ 1.16 (t, 3H), 2.57 (q, 2H), 3.66 (s, 2H), 7.22 (d, 1H), 7.56 (dd, 1H), 8.31 (d, 1H), 12.44 (br s, 1H).

후처리

  1. custombefore removing the volatiles in vacuo
  2. additionWater was added
  3. dissolutionto dissolve the solids
  4. washThe solution was washed with 2-methylTHF (2×)
  5. concentrationwas concentrated under vacuum to an oily solid
  6. customThe residue was triturated with hot chloroform and heptanes

출처 및 근거

ORD 기록
ord-d6af2b421568465d961fb9ca6af53cff
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08609680B2

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