Sodium Bicarbonate → 3-[1-(2-Pyridinylmethyl)-2-pyrrolidinyl]phenol

HRID 742578노트

반응식

HRID 742578 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH:9]2[CH2:13][CH2:12][CH2:11][N:10]2[CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=2)[CH:6]=[CH:7][CH:8]=1.C(=O)(O)[O-].[Na+]>Br>[N:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[CH2:14][N:10]1[CH2:11][CH2:12][CH2:13][CH:9]1[C:5]1[CH:4]=[C:3]([OH:2])[CH:8]=[CH:7][CH:6]=1

참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 233612632-(3-Methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidine

생성물 1

HCID 233613143-[1-(2-Pyridinylmethyl)-2-pyrrolidinyl]phenol수율 69%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

2-(3-Methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidine and 48% hydrobromic acid (40 ml) were warmed to 100° C. for 7 hrs, cooled to ambient temperature, and neutralized with saturated sodium bicarbonate solution. The mixture was extracted with dichloromethane (2 times). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, 1:1 ethyl acetate/dichloromethane). The appropriate fractions were collected and concentrated to give 2.7 g (69%) of product, mp 96°-98° C.

후처리

  1. extractionThe mixture was extracted with dichloromethane (2 times)
  2. dry with materialThe combined organic extracts were dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated
  5. customThe residue was purified by flash column chromatography (silica gel, 1:1 ethyl acetate/dichloromethane)
  6. customThe appropriate fractions were collected
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-54121325f6c4430199518ae2bc9af48d
출처 데이터셋
uspto-grants-1996_09
특허 번호
US05554750

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