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Hydrochloric Acid → 2,2-Difluoro-benzo(1,3)dioxole-4-carbaldehyde

HRID 476977
Notes
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Reaction equation

HRID 476977 reaction equation
Br[CH2:2][C:3]1[C:11]2[O:10][C:9]([F:13])([F:12])[O:8][C:7]=2[CH:6]=[CH:5][CH:4]=1.C1N2CN3CN(C2)CN1C3.Cl.[OH2:25]>>[F:12][C:9]1([F:13])[O:8][C:7]2[CH:6]=[CH:5][CH:4]=[C:3]([CH:2]=[O:25])[C:11]=2[O:10]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 962Water2×HCID 4101HexamethylenetetramineHCID 109994864-(Bromomethyl)-2,2-difluoro-1,3-dioxaindane

Product 1

HCID 27369702,2-Difluoro-benzo(1,3)dioxole-4-carbaldehyde

Procedure

117 g of crude 4-bromomethyl-2,2-difluoro-1,3-benzodioxole are added to 120 g of urotropin in 250 ml of water and the mixture is heated under reflux for 3 hours. 120 ml of hydrochloric acid in 150 ml of water are then added and the mixture is heated for a further 3 hours. The crude product is then driven over with steam, removed from the receiver and shaken with 100 g of sodium bisulphate in 250 ml of water. After extraction with methylene chloride, the aqueous phase is acidified with 2N sulphuric acid and the aldehyde is separated off and distilled. The yield is 53 g.

Workup

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 3 hours
  3. temperaturethe mixture is heated for a further 3 hours
  4. customremoved from the receiver
  5. extractionAfter extraction with methylene chloride
  6. customthe aldehyde is separated off
  7. distillationdistilled

Sources & evidence

ORD record
ord-f4f080cea95240928f74e252c3352113
Source dataset
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04886816

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes