Potassium Cyanide → HCID 21450274, compound

HRID 596703Notes

Reaction equation

HRID 596703 reaction equation
N[C:2]1[CH:14]=[CH:13][C:5]([C:6]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[O:7])=[CH:4][C:3]=1[O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.N([O-])=O.[Na+].[C-:27]#[N:28].[K+]>Cl>[CH2:16]([O:15][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][C:2]=1[C:27]#[N:28])[C:6]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[O:7])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

5

Reactant 3

HCID 9032Potassium CyanideHCID 21450248HCID 21450248, compoundHCID 23668193Sodium Nitrite

Product 1

HCID 21450274HCID 21450274, compound

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

3-(4-Amino-3-benzyloxybenzoyl)propionic acid was diazotised in aqueous hydrochloric acid with sodium nitrite and the resultant solution was treated with cuprous cyanide in aqueous potassium cyanide solution to give 3-(3-benzyloxy-4-cyanobenzoyl)propionic acid.

Sources & evidence

ORD record
ord-73b2de5caf3741b08f4abea50c7f50d9
Source dataset
uspto-grants-1977_03
Patent number
US04011321

Reaction notes

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