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

Hydrochloric Acid → 5-Cyanopentanoic acid

HRID 581651
Notes
Print preview

Reaction equation

HRID 581651 reaction equation
[NH4+].[C:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]([O-:10])=[O:9])#[N:3].Cl>>[C:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9])#[N:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 19044055HCID 19044055, compound

Product 1

HCID 1999265-Cyanopentanoic acidYield 95%

Procedure

A 200-mL portion of the filtrate of the product mixture described above, containing the 5-cyanopentanoic acid ammonium salt (1.13M), was adjusted to pH 2.5 with 6 N HCl, then saturated with sodium chloride and extracted with 4×200 mL of ethyl ether. The combined ether extracts were dried over magnesium sulfate, filtered, and the solvent removed by rotary evaporation at reduced pressure. Remaining ether was removed by stirring the colorless liquid at room temperature under high vacuum (60 millitorr) for 5 h to yield 27.32 g (95% isolated yield) of 5-cyanopentanoic acid. The 5-cyanopentanoic acid was then distilled under vacuum (75 millitorr) at 110-112° C. without decomposition.

Workup

  1. extractionsaturated with sodium chloride and extracted with 4×200 mL of ethyl ether
  2. dry with material
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
The combined ether extracts were dried over magnesium sulfate
  • filtrationfiltered
  • customthe solvent removed by rotary evaporation at reduced pressure
  • customRemaining ether was removed
  • Sources & evidence

    ORD record
    ord-358a96e5f95b4ca295c5555a036be20c
    Source dataset
    uspto-grants-1999_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05922589

    Reaction notes

    Loading…