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2,4-Dichloropyrimidine-5-carbaldehyde → 1-(2,4-Dichloropyrimidin-5-yl)ethan-1-ol

HRID 750484
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인쇄 미리보기

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HRID 750484 반응식
[Cl:1][C:2]1[N:7]=[C:6]([Cl:8])[C:5]([CH:9]=[O:10])=[CH:4][N:3]=1.[CH3:11][Mg]Br>C1COCC1>[Cl:1][C:2]1[N:7]=[C:6]([Cl:8])[C:5]([CH:9]([OH:10])[CH3:11])=[CH:4][N:3]=1
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참가 물질

4

반응물 2

HCID 189831682,4-Dichloropyrimidine-5-carbaldehydeHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 151416481-(2,4-Dichloropyrimidin-5-yl)ethan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

To a stirred solution of 2,4-dichloro-pyrimidine-5-carbaldehyde (Example 17, 1.01 g, 5.7 mmol) in THF (10 mL), methyl magnesium bromide (Aldrich, 3 M in ether, 6.27 mmol, 2.1 mL) was added slowly at −78° C. The mixture was stirred for an additional 2 hours at −78° C. and the reaction was quenched with 1N HCl (10 mL). The resulting mixture was extracted with EtOAc and the extract was dried with sodium sulfate. Removal of solvent gave a brown solid. 1.07 g, 97%. MS (M+H)+, 193.

후처리

  1. customthe reaction was quenched with 1N HCl (10 mL)
  2. extractionThe resulting mixture was extracted with EtOAc
  3. dry with materialthe extract was dried with sodium sulfate
  4. customRemoval of solvent
  5. customgave a brown solid

출처 및 근거

ORD 기록
ord-f0dabc8583a943b48fa5f0303b1eebc3
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07405220B2

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