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4-Methoxybenzalcyanoacetic acid → 2-Cyano-3-(4-methoxyphenyl)propanoic acid

HRID 1905733
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HRID 1905733 반응식
[BH4-].[Na+].[C:3]([C:5](=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=1)[C:6]([OH:8])=[O:7])#[N:4]>C([O-])(O)=O.[Na+].CO>[C:3]([CH:5]([CH2:9][C:10]1[CH:11]=[CH:12][C:13]([O:16][CH3:17])=[CH:14][CH:15]=1)[C:6]([OH:8])=[O:7])#[N:4]
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참가 물질

5

반응물 2

HCID 2332604-Methoxybenzalcyanoacetic acidHCID 4311764Sodium borohydride

생성물 1

HCID 137111482-Cyano-3-(4-methoxyphenyl)propanoic acid

시약·촉매·용매 2

HCID 887Methanol용매HCID 516892Sodium Bicarbonate용매

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온도
15 °C

실험 절차

Sodium borohydride (30.2 g) is added portionwise over a period of 2 hours to a stirred mixture of α-cyano-4-methoxycinnamic acid (52.5 g) in aqueous saturated NaHCO3 (200 ml) and methanol (600 ml) cooled to about 15° C. The reaction mixture is allowed to warm to RT, stirred at RT for 30 min and concentrated in vacuo. The residue is partitioned between water and ether and the aqeuous layer acidified and extracted with ether. The ether extract is washed, dried over Na2SO4, filtered and the filtrate evaporated in vacuo producing a liquid which is crystallized from toluene yielding the desired product as a solid, M.P. 94°-95° C.

후처리

  1. temperatureto warm to RT
  2. concentrationconcentrated in vacuo
  3. customThe residue is partitioned between water and ether
  4. extractionextracted with ether
  5. extractionThe ether extract
  6. washis washed
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customthe filtrate evaporated in vacuo
  10. customproducing a liquid which
  11. customis crystallized from toluene yielding the desired product as a solid, M.P. 94°-95° C.

출처 및 근거

ORD 기록
ord-80228c2ffa024112afd2c3ffed7585c6
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04647559

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