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Hydrochloric Acid → (5-Methoxypyridazin-3-yl)methanol

HRID 891946
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HRID 891946 반응식
C([O:3][C:4]([C:6]1[N:7]=[N:8][CH:9]=[C:10]([O:12][CH3:13])[CH:11]=1)=O)C.[BH4-].[Na+].Cl.C(=O)(O)[O-].[Na+]>C(O)C>[CH3:13][O:12][C:10]1[CH:11]=[C:6]([CH2:4][OH:3])[N:7]=[N:8][CH:9]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 23600258Ethyl 5-methoxypyridazine-3-carboxylate

생성물 1

HCID 22240192(5-Methoxypyridazin-3-yl)methanol수율 83.4%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

5-Methoxy-pyridazine-3-carboxylic acid ethyl ester (8.1 g, 44.5 mmol) was dissolved in ethanol (105 ml) under argon. The reaction mixture was cooled to 0° C. and treated with NaBH4 (3.5 g, 89 mmol). After 10 minutes, the reaction mixture was warmed to room temperature, stirred for 1 hour and treated successively with 2N HCl and saturated sodium bicarbonate to adjust the pH at 8. The solvent was removed in vacuo and the residue was stirred with MeOH (100 ml). The suspension was filtered and the filtrate was concentrated. The residue was chromatographed over silica gel (CH2Cl2—MeOH 19:1) to provide (5-methoxy-pyridazin-3-yl)-methanol (5.2 g, 83%) as a light brown solid, MS: m/e=140 (M+).

후처리

  1. temperaturethe reaction mixture was warmed to room temperature
  2. customThe solvent was removed in vacuo
  3. stirringthe residue was stirred with MeOH (100 ml)
  4. filtrationThe suspension was filtered
  5. concentrationthe filtrate was concentrated
  6. customThe residue was chromatographed over silica gel (CH2Cl2—MeOH 19:1)

출처 및 근거

ORD 기록
ord-f6aeae6adc7f4e68a6cb71a2ab701636
출처 데이터셋
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07005432B2

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