Sodium Bicarbonate → 5-Chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid

HRID 637681노트

반응식

HRID 637681 반응식
[Cl:1][C:2]1[C:3]([N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=[CH:4][C:5]([O:12]C)=[C:6]([CH2:8][C:9]([OH:11])=[O:10])[CH:7]=1.C(=O)(O)[O-].[Na+]>Br.O>[Cl:1][C:2]1[C:3]([N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=[CH:4][C:5]([OH:12])=[C:6]([CH2:8][C:9]([OH:11])=[O:10])[CH:7]=1

참가 물질

5

반응물 2

HCID 516892Sodium BicarbonateHCID 541834705-Chloro-2-methoxy-4-(piperidin-1-yl)-phenylacetic acid

생성물 1

HCID 539130445-Chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid

시약·촉매·용매 2

HCID 260Hydrogen Bromide용매HCID 962Water용매

실험 절차

A solution of 8.5 g (30 mmole) of 5-chloro-2-methoxy-4-(piperidin-1-yl)-phenylacetic acid in 150 ml of 48% hydrobromic acid is boiled under reflux for 15 hours. The reaction mixture is cooled, diluted with water and adjusted to pH 3-4 with saturated sodium bicarbonate solution. The whole is subsequently extracted with ethyl acetate and the combined organic phases are washed with water, dried over sodium sulphate and concentrated by evaporation in a vacuum rotary evaporator. In that manner a dark grey foam of 5-chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid is obtained which is reacted, without purification, to form 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one.

후처리

  1. temperatureunder reflux for 15 hours
  2. temperatureThe reaction mixture is cooled
  3. extractionThe whole is subsequently extracted with ethyl acetate
  4. washthe combined organic phases are washed with water
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated by evaporation in a vacuum rotary evaporator

출처 및 근거

ORD 기록
ord-7452b70b0ab14af28daffa3c840e9f0b
출처 데이터셋
uspto-grants-1985_12
특허 번호
US04558043

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