Ethanol → HCID 20242606, compound

HRID 483140Notes

Reaction equation

HRID 483140 reaction equation
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH2:10][C:11]#[N:12])=[CH:4][C:3]=2[O:2]1.[Cl:13][C:14]1[CH:21]=[CH:20][CH:19]=[CH:18][C:15]=1[CH:16]=O.C([OH:24])C>>[Cl:13][C:14]1[CH:21]=[CH:20][CH:19]=[CH:18][C:15]=1[CH:16]1[C:6]2[C:5](=[CH:4][C:3]3[O:2][CH2:1][O:9][C:8]=3[CH:7]=2)[CH2:10][C:11](=[O:24])[NH:12]1

Participants

4

Reactant 3

HCID 702EthanolHCID 69962-ChlorobenzaldehydeHCID 781783,4-(Methylenedioxy)phenylacetonitrile

Product 1

HCID 20242606HCID 20242606, compound

Procedure

This compound was prepared in an analogous manner to that described in DESCRIPTION 18, from 3,4-methylenedioxyphenylacetonitile and 2-chlorobenzaldehyde. m.p. 207°-9° C. (Ethanol).

Workup

  1. customThis compound was prepared in an analogous manner to that

Sources & evidence

ORD record
ord-74966ffe3c4842ca8925af2003fa0f1d
Source dataset
uspto-grants-1986_03
Patent number
US04578393

Reaction notes

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