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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 85189178, 화합물

HRID 1184297
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인쇄 미리보기

반응식

HRID 1184297 반응식
C([O:5][C:6](=[O:24])[CH2:7][CH2:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH:20]=[CH:21][CH2:22][Br:23])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[Br:23][CH2:22][CH:21]=[CH:20][CH2:19][O:18][CH2:17][CH2:16][O:15][CH2:14][CH2:13][O:12][CH2:11][CH2:10][O:9][CH2:8][CH2:7][C:6]([OH:24])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 53399024tert-Butyl 17-bromo-4,7,10,13-tetraoxaheptadec-15-en-1-oate

생성물 1

HCID 85189178HCID 85189178, 화합물수율 98.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

At RT, a solution of 1 g of 3-(2-{2-[2-(4-bromo-but-2-enyloxy)-ethoxy]-ethoxy}-ethoxy)-propionic acid tert-butyl ester (commercially available), 6 ml of TFA and 3 ml of DCM is stirred during 3 hrs, and then concentrated to dryness under RP. The oily residue is diluted with toluene and concentrated to dryness under RP affording 853 mg of 3-(2-{2-[2-(4-bromo-but-2-enyloxy)-ethoxy]-ethoxy}-ethoxy)-propionic acid in the form of a brown oil.

후처리

  1. concentrationconcentrated to dryness under RP
  2. additionThe oily residue is diluted with toluene
  3. concentrationconcentrated to dryness under RP

출처 및 근거

ORD 기록
ord-e50903a50cdf4bbfb7f7e6ef1db14eda
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08668910B2

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