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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetonitrile → HCID 118108924, 화합물

HRID 716161
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반응식

HRID 716161 반응식
C(#N)C.Cl.[CH3:5][O:6][NH2:7].[C:8]1([CH:14]2[O:18][CH:17](O)[CH2:16][CH2:15]2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>O.C(OCC)(=O)C.CCCCCC.C(N(CC)CC)C>[CH3:5][O:6][N:7]=[CH:17][CH2:16][CH2:15][CH:14]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 6342AcetonitrileHCID 521874O-Methylhydroxylamine hydrochlorideHCID 111163882-Furanol, tetrahydro-5-phenyl-

생성물 1

HCID 118108924HCID 118108924, 화합물수율 95.4%

시약·촉매·용매 4

HCID 962Water용매2회HCID 8058Hexane용매
HCID 8471
Triethylamine
용매
HCID 8857Ethyl Acetate용매

실험 절차

12 mL of acetonitrile, 6 mL of water and 1.0 g of O-methylhydroxylamine hydrochloride were added to 0.98 g of the 5-phenyloxolan-2-ol, and thereafter, 1.08 mL of triethylamine was added dropwise to the mixture. The thus obtained mixture was stirred at room temperature for 0.5 hours. Thereafter, hexane, ethyl acetate and water were added to the reaction mixture, and the water layer was then removed. The organic layer was dried over anhydrous sodium sulfate. After that, the solvent was distilled away under reduced pressure, so as to obtain 1.10 g of 4-(methoxyimino)-1-phenylbutan-1-ol in the form of a colorless oily product.

후처리

  1. customthe water layer was then removed
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. distillationAfter that, the solvent was distilled away under reduced pressure

출처 및 근거

ORD 기록
ord-0216562d95584f6f97f51e2f82b3412a
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187514B2

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