HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Hydrochloric Acid → HCID 85875172, compound

HRID 643195
Notes
Print preview

Reaction equation

HRID 643195 reaction equation
C(=O)([O-])O.[K+].Cl[CH2:7][C:8]([NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[O:9].[C-:19]#[N:20].[K+].Cl>O>[C:19]([CH2:7][C:8]([NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[O:9])#[N:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 9032Potassium CyanideHCID 516893Potassium BicarbonateHCID 21040516-(2-Chloroacetamido)hexanoic acid

Product 1

HCID 85875172HCID 85875172, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

2.8 g (20 mmol) potassium hydrogen carbonate were added to 8.3 g (40 mmol) 6-(chloracetamido) hexanoic acid dissolved in 25 ml water. 3.2 g (48 mmol) potassium cyanide was then added to the clear solution which was cooled on ice. The reaction mixture was stirred for 17 hours and was then acidified with HCl (2N). The residue after extraction was purified by chromatography (silica gel, solvent: ethyl acetate).

Workup

  1. temperaturewas cooled on ice
  2. extractionThe residue after extraction
  3. customwas purified by chromatography (silica gel, solvent: ethyl acetate)

Sources & evidence

ORD record
ord-89a04f08e9d6410690e8f9eb18855139
Source dataset
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07700306B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes