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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 3-(5-Methyl-1,3,4-oxadiazol-2-yl)phenol

HRID 1798801
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인쇄 미리보기

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HRID 1798801 반응식
COC1C=CC(C[O:8][C:9]2[CH:10]=[C:11]([C:15]3[O:16][C:17]([CH3:20])=[N:18][N:19]=3)[CH:12]=[CH:13][CH:14]=2)=CC=1.C(O)(C(F)(F)F)=O>>[CH3:20][C:17]1[O:16][C:15]([C:11]2[CH:10]=[C:9]([OH:8])[CH:14]=[CH:13][CH:12]=2)=[N:19][N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 58128485HCID 58128485, 화합물

생성물 1

HCID 129617433-(5-Methyl-1,3,4-oxadiazol-2-yl)phenol

실험 절차

2-{3-[(4-Methoxybenzyl)oxy]phenyl}-5-methyl-1,3,4-oxadiazole (100 mg, 0.338 mmol) was treated with 0.5 mL TFA and was stirred at room temperature for 10 min. Excess TFA was removed under vacuum and the residue was purified by column chromatography using a 24 gram biotage silica gel cartridge eluting with 20-50% ethyl acetate/hexanes (gradient) to give the product as white solid. LRMS calc: 176.1; obs: 177.2 (M+1).

후처리

  1. customExcess TFA was removed under vacuum
  2. customthe residue was purified by column chromatography
  3. washeluting with 20-50% ethyl acetate/hexanes (gradient)

출처 및 근거

ORD 기록
ord-e5db634352fa4d798eb663fcfaa7623b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343990B2

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