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Potassium Carbonate → 3-(2-(7-Bromoquinolin-2-yl)-ethynyl)phenol

HRID 1088463
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반응식

HRID 1088463 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]#[C:13][C:14]3[CH:15]=[C:16]([CH:22]=[CH:23][CH:24]=3)[O:17]CC([O-])=O)=[N:9]2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.CO>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]#[C:13][C:14]3[CH:15]=[C:16]([OH:17])[CH:22]=[CH:23][CH:24]=3)=[N:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 221630983-(2-(7-Bromoquinolin-2-yl)-ethynyl)phenoxyacetate

생성물 1

HCID 104714733-(2-(7-Bromoquinolin-2-yl)-ethynyl)phenol

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of the acetate from Step 2 (550 mg) in THF (5 mL) and methanol (5 mL) was added milled potassium carbonate (414 mg) and the mixture stirred at room temperature for 2.5 hours. The mixture was poured into pH 7 buffer solution and extracted with ethyl acetate. The organic layer was dried, filtered and filtrate evaporated to afford the title product as yellow-solid: m.p. 197°-199° C.

후처리

  1. extractionextracted with ethyl acetate
  2. customThe organic layer was dried
  3. filtrationfiltered
  4. customfiltrate evaporated

출처 및 근거

ORD 기록
ord-aead6ba9cfdc4802809a7d291aeb5454
출처 데이터셋
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04962203

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