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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonia → HCID 13674881, 화합물

HRID 1650000
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인쇄 미리보기

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HRID 1650000 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][CH2:10][CH:11]([N:13]([CH3:15])[CH3:14])[CH3:12].[CH:16](O)=O.C=O.N>O>[CH3:16][N:9]([CH2:10][CH:11]([N:13]([CH3:15])[CH3:14])[CH3:12])[C:3]1[C:2]([CH3:1])=[CH:7][CH:6]=[CH:5][C:4]=1[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 284Formic AcidHCID 712FormaldehydeHCID 134365Gyki 23107

생성물 1

HCID 13674881HCID 13674881, 화합물수율 98%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 1.5 g (7.3 mmoles) of 1-(2,6-dimethylphenyl-amino)-2-dimethylamino-propane, prepared as described in Example 8, 1.5 ml of 99% formic acid and 1.5 ml of a 36% aqueous formaldehyde solution is boiled for 6 hours. The mixture is cooled, poured onto 30 ml of water, the aqueous solution is rendered alkaline (pH=9) with concentrated aqueous ammonia, and extracted then thrice with 10 ml of benzene, each. The benzene solutions are combined, dried over anhydrous potassium carbonate, and the solvent is evaporated under reduced pressure. 1.58 g (98,8%) of 1-[N-methyl-N-(2,6-dimethylphenyl)-amino]2-dimethylamino-propane are obtained as a light yellow oil; b.p.: 102°-104° C./133.3 Pa.

후처리

  1. customprepared
  2. temperatureThe mixture is cooled
  3. extractionextracted
  4. dry with materialdried over anhydrous potassium carbonate
  5. customthe solvent is evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-76d1e5a0e29b41858160b212e96d8476
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04922021

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