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Sodium Cyanide → Cyano(2,4-dioxo-1-propargyl-3-imidazolidinyl)methanol

HRID 2050346
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반응식

HRID 2050346 반응식
[O:1]=[C:2]1[N:6]([CH:7]=[O:8])[C:5](=[O:9])[CH2:4][N:3]1[CH2:10][C:11]#[CH:12].[C-:13]#[N:14].[Na+].S(=O)(O)[O-].[Na+]>CCOCC.O>[C:13]([CH:7]([N:6]1[C:5](=[O:9])[CH2:4][N:3]([CH2:10][C:11]#[CH:12])[C:2]1=[O:1])[OH:8])#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8929Sodium CyanideHCID 203426582,4-Dioxo-1-propargyl-3-imidazolidine-carbaldehydeHCID 23665763Sodium Bisulfite

생성물 1

HCID 20342650Cyano(2,4-dioxo-1-propargyl-3-imidazolidinyl)methanol

시약·촉매·용매 2

HCID 962Water용매2회HCID 3283Diethyl Ether용매

실험 절차

To a solution of 2,4-dioxo-1-propargyl-3-imidazolidine-carbaldehyde (1.8 mmol) in 25 ml of ether is added 25 ml of water followed by sodium cyanide (3.04 mmol). The mixture is stirred vigorously while a solution of sodium bisulfite (2.45 mmol) in 15 ml of water is added over about 5 minutes. The reaction mixture is stirred for two hours. The organic phase is separated, washed with water, dried over calcium sulfate and solvent evaporated to give cyano(2,4-dioxo-1-propargyl-3-imidazolidinyl)methanol.

후처리

  1. additionis added over about 5 minutes
  2. customThe organic phase is separated
  3. washwashed with water
  4. dry with materialdried over calcium sulfate and solvent
  5. customevaporated

출처 및 근거

ORD 기록
ord-bd696feb11a6475790143d41b9c225f4
출처 데이터셋
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04200758

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