1-Naphthaldehyde → HCID 56617092, compound
Reaction equation
[C:1]1(C=O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH2:13]([O:15][C:16](=[O:22])[CH2:17][C:18]([CH2:20][Cl:21])=[O:19])[CH3:14]>>[CH2:13]([O:15][C:16](=[O:22])[C:17](=[C:3]1[CH:2]=[CH:1][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4]1)[C:18](=[O:19])[CH2:20][Cl:21])[CH3:14]Participants
3
Procedure
9.85 g of 1-naphthaldehyde were reacted with 15.2 g of 4-chloroacetoacetic acid ethyl ester in the course of 10 hours as described in Example 24. After incipient distillation under a high vacuum had been carried out, a 2:1 isomer mixture which still contained traces of aldehyde remained as the residue.
Workup
- distillationAfter incipient distillation under a high vacuum
Sources & evidence
- ORD record
- ord-5fcea39303c7496fa3b21e2f064813b6
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04416880
Reaction notes
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