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Formaldehyde → Ethyl (1-phenyl-1,3-diazaspiro[4.5]dec-3-yl)acetate

HRID 1894854
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인쇄 미리보기

반응식

HRID 1894854 반응식
[C:1]1([NH:7][C:8]2([CH2:14][NH:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:22]=O>ClCCl>[C:1]1([N:7]2[C:8]3([CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]3)[CH2:14][N:15]([CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:22]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 712FormaldehydeHCID 86646976Ethyl [(1-phenylaminocyclohexylmethyl)amino]acetate

생성물 1

HCID 86646977Ethyl (1-phenyl-1,3-diazaspiro[4.5]dec-3-yl)acetate수율 98%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
100 °C

실험 절차

510 mg (1.75 mmol) of ethyl [(1-phenylaminocyclohexylmethyl)amino]-acetate are dissolved in 10 ml of dichloromethane and 10 ml of formaldehyde are added. The solution is heated to 100° C. with microwaves for 30 min. The medium is poured into dichloromethane and washed with water. The organic phases are collected and then dried over sodium sulfate. The solvents are evaporated. 520 mg of ethyl (1-phenyl-1,3-diazaspiro[4.5]dec-3-yl)acetate are obtained in the form of a colorless oil. Yield=98%.

후처리

  1. washwashed with water
  2. customThe organic phases are collected
  3. dry with materialdried over sodium sulfate
  4. customThe solvents are evaporated

출처 및 근거

ORD 기록
ord-5916c4f0847f4571a3cdd3f5e3cdb214
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08513307B2

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