HCID 13486522, compound → HCID 21539909, compound

HRID 1076339Notes

Reaction equation

HRID 1076339 reaction equation
C([C:3]1[CH:10]=[CH:9][C:6]([CH2:7]Cl)=[CH:5][C:4]=1F)#N.[C:12]([O:15]C1C=CC(CCl)=CC=1F)(=[O:14])[CH3:13].C(NC1C=CC(CCl)=CC=1F)(=O)C.C(C1C=CC(CCl)=CC=1OC)#N.C(C1C=C(C=CC=1N(C)C)CCl)#N.C(NC1C=CC(CCl)=CC=1OC)(=O)C.[C:77]([O:85]C1C=CC(CCl)=CC=1)(=[O:84])[C:78]1[CH:83]=CC=CC=1.C(NC1C=CC(CCl)=CC=1)(=O)C1C=CC=CC=1>>[CH3:83][CH:78]([CH2:7][C:6]1[CH:5]=[CH:4][C:3]([O:15][C:12](=[O:14])[CH3:13])=[CH:10][CH:9]=1)[C:77]([OH:85])=[O:84]

Participants

9

Reactant 8

HCID 13486522HCID 13486522, compoundHCID 21539900HCID 21539900, compoundHCID 21539901HCID 21539901, compoundHCID 21539930HCID 21539930, compoundHCID 21539953HCID 21539953, compoundHCID 21539961HCID 21539961, compoundHCID 54475202HCID 54475202, compoundHCID 55274592HCID 55274592, compound

Product 1

HCID 21539909HCID 21539909, compound

Procedure

Similarly, when p-cyano-m-fluorobenzylchoride, p-acetyloxy-m-fluorobenzylchloride, p-acetylamino-m-fluorobenzylchloride, p-cyano-m-methoxybenzylchloride, m-cyano-p-dimethylaminobenzylchloride, p-cyano-O-fluorobenzylchloride, p-acetylamino-m-methoxybenzylchloride, p-benzoyloxybenzylchloride, p-benzoylaminobenzylchloride, m,p-dicyanobenzylchloride, m,p-diacetylaminobenzylchloride, or m,p-diacetyloxybenzylchloride is used in place of p-cyanobenzylchloride, there is obtained

Workup

  1. customthere is obtained

Sources & evidence

ORD record
ord-a70fc23f173f4d9799d4d79f7562e464
Source dataset
uspto-grants-1976_05
Patent number
US03956363

Reaction notes

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