Acetic Acid → Formaldehyde

HRID 1447142Notes

Reaction equation

HRID 1447142 reaction equation
[Br:1][C:2]1[C:15]2[C:16]3=[C:17]4[C:12](=[CH:13][CH:14]=2)[CH:11]=[CH:10][CH:9]=[C:8]4[CH:7]=[CH:6][C:5]3=[CH:4][CH:3]=1.[C:18](O)(=[O:20])C>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:16]3=[C:17]4[C:8]([CH:9]=[CH:10][CH:11]=[C:12]4[CH:13]=[CH:14][C:15]=13)=[CH:7][CH:6]=2.[CH2:18]=[O:20]

Participants

4

Reactant 2

HCID 176Acetic AcidHCID 1596271-Bromopyrene

Product 2

HCID 712FormaldehydeHCID 1596271-Bromopyrene

Procedure

Another photoconductor material used was bromopyrene resin. This product is obtained by condensation of 3-bromopyrene, melting point 94° to 95° C. (Organic Synthesis, Vol. 48 (1968), page 30) with formaldehyde in glacial acetic acid.

Sources & evidence

ORD record
ord-042d12dbac5547359e0ac8070fd80528
Source dataset
uspto-grants-1982_02
Patent number
US04315981

Reaction notes

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