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Sodium Nitrite → HCID 53907140, compound

HRID 2051859
Notes
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Reaction equation

HRID 2051859 reaction equation
[Cl:1][CH2:2][CH2:3][NH:4][C:5]([N:7]([CH2:13][CH2:14][CH3:15])[CH2:8][CH:9]([OH:12])[CH2:10][OH:11])=[O:6].[N:16]([O-])=[O:17].[Na+]>C(O)(=O)C>[Cl:1][CH2:2][CH2:3][N:4]([N:16]=[O:17])[C:5]([N:7]([CH2:13][CH2:14][CH3:15])[CH2:8][CH:9]([OH:12])[CH2:10][OH:11])=[O:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 23668193Sodium NitriteHCID 54573596N′-(2-Chloroethyl)-N-(2,3-dihydroxypropyl)-N-propylurea

Product 1

HCID 53907140HCID 53907140, compoundYield 50.5%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

3 g 1-(2-chloroethyl)-3-n-propyl-3-(2,3-dihydroxy-n-propyl)urea are dissolved in 10 ml of acetic acid, and 1.5 g of sodium nitrite are added thereto under stirring. The mixture is stirred at the same temperature for 4 hours. After the reaction, the mixture is treated in the same manner as described in Example 62-(2). 1.7 g of 1-(2-chloroethyl)-1-nitroso-3-n-propyl-3-(2,3-dihydroxy-n-propyl)urea are thereby obtained as a yellow oil.

Workup

  1. stirringThe mixture is stirred at the same temperature for 4 hours
  2. customAfter the reaction
  3. additionthe mixture is treated in the same manner

Sources & evidence

ORD record
ord-ada6c0d12f094d68bbc7232fc7fd77a7
Source dataset
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04182757

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes