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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pyridine → Trimethylsilyl crotonate

HRID 1246288
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HRID 1246288 반응식
N1C=CC=CC=1.[C:7]([OH:12])(=[O:11])/[CH:8]=[CH:9]/[CH3:10].Cl[Si:14]([CH3:17])([CH3:16])[CH3:15]>CCOCC>[CH3:15][Si:14]([O:11][C:7](=[O:12])/[CH:8]=[CH:9]/[CH3:10])([CH3:17])[CH3:16]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 6397ChlorotrimethylsilaneHCID 637090Crotonic Acid

생성물 1

HCID 5702560Trimethylsilyl crotonate수율 79%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Pyridine (138 g, 1.74 mol) is added dropwise to a stirred solution of crotonic acid (125 g, 1.45 mol), and chlorotrimethylsilane (189 g 1.74 mol) in ether (1.5 l) at room temperature. The reaction mixture is allowed to stir at room temperature overnight and the precipitate is removed by filtration. The filtrate is concentrated and the residue is distilled under reduced pressure. The product fraction is collected at 58–70° C. (25 mmHg) to give 180 g of the title compound (79%). GC-MS purity is 93.4%, 1HNMR is consistent with the structure.

후처리

  1. customthe precipitate is removed by filtration
  2. concentrationThe filtrate is concentrated
  3. distillationthe residue is distilled under reduced pressure
  4. customThe product fraction is collected at 58–70° C. (25 mmHg)

출처 및 근거

ORD 기록
ord-0a1609a66b9f4e61b41fe5763184c4d9
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07126025B2

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