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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydroxyamine hydrochloride → HCID 86659950, 화합물

HRID 1804521
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HRID 1804521 반응식
[CH3:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1.Cl.[NH2:15][OH:16].C(=O)(O)[O-].[Na+]>CO>[OH:16][N:15]=[C:6]([NH2:7])[C:5]1[CH:8]=[CH:9][C:2]([CH3:1])=[CH:3][C:4]=1[C:10]([F:13])([F:11])[F:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 27755974-Methyl-2-(trifluoromethyl)benzonitrile

생성물 1

HCID 86659950HCID 86659950, 화합물수율 45.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

An oven-dried 20 mL reaction vial containing a stir bar was cooled under a stream of dry nitrogen. The vial was charged with 4-methyl-2-(trifluoromethyl)benzonitrile (1000 mg, 5.40 mmol), hydroxylamine hydrochloride (469 mg, 6.75 mmol), sodium bicarbonate (681 mg, 8.10 mmol), and methanol (6 mL). The vial was flushed with nitrogen, sealed, stirred at room temperature for 30 minutes, and then placed in a sand bath set to 75° C. and stirred overnight. The crude reaction material was purified by reverse phase preparative HPLC. The collected product fractions were evaporated under vacuum to afford N′-hydroxy-4-methyl-2-(trifluoromethyl)benzimidamide (0.54 g, 2.45 mmol, 45% yield). MS M+1=219.0.

후처리

  1. customAn oven-dried 20 mL reaction
  2. additionvial containing a stir bar
  3. temperaturewas cooled under a stream of dry nitrogen
  4. customThe vial was flushed with nitrogen
  5. customsealed
  6. customplaced in a sand bath
  7. customset to 75° C.
  8. stirringstirred overnight
  9. customThe crude reaction material
  10. customwas purified by reverse phase preparative HPLC
  11. customThe collected product fractions were evaporated under vacuum

출처 및 근거

ORD 기록
ord-2c8cbcfb06914b3baf4cd253207fcdfb
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354398B2

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