홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ammonium Hydroxide → 3,3,3-Trifluoro-2,2-dimethyl-propionamide

HRID 1049291
노트
인쇄 미리보기

반응식

HRID 1049291 반응식
[F:1][C:2]([F:10])([F:9])[C:3]([CH3:8])([CH3:7])[C:4](O)=[O:5].C(Cl)(=O)C(Cl)=O.[NH4+:17].[OH-]>C(Cl)Cl.CN(C=O)C.C1COCC1>[F:1][C:2]([F:10])([F:9])[C:3]([CH3:8])([CH3:7])[C:4]([NH2:17])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 14923Ammonium HydroxideHCID 65578Oxalyl chlorideHCID 198673673,3,3-Trifluoro-2,2-dimethylpropanoic acid

생성물 1

HCID 575162793,3,3-Trifluoro-2,2-dimethyl-propionamide수율 74.5%

시약·촉매·용매 3

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane
용매
HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 3,3,3-trifluoro-2,2-dimethylpropionic acid (0.5 g, 3.20 mmol) in DCM (5 mL) was treated with oxalyl chloride (0.350 mL, 4.00 mmol) and 1 drop of DMF, stirred at RT for 1 h, added drop-wise to a solution of NH4OH (˜15M, 5 mL, ˜75 mmol) in THF (5 mL) and stirred at RT overnight. Solids were removed via filtration through diatomaceous earth, rinsed well with 4:1 DCM/THF, the filtrate saturated with solid NaCl, extracted with 4:1 DCM/THF (3×) and the combined organics were dried over Na2SO4 and concentrated to dryness to afford 3,3,3-trifluoro-2,2-dimethylpropanamide (370 mg, 74%). 1H NMR (400 MHz, DMSO-d6): δ 7.42 (s, 1H), 7.35 (s, 1H), 1.29 (s, 6H).

후처리

  1. stirringstirred at RT overnight
  2. customSolids were removed via filtration through diatomaceous earth
  3. washrinsed well with 4:1 DCM/THF
  4. extractionthe filtrate saturated with solid NaCl, extracted with 4:1 DCM/THF (3×)
  5. dry with materialthe combined organics were dried over Na2SO4
  6. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-08afd0753be84632831fa4db7b803dcb
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382228B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트