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

HRID 476977
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반응식

HRID 476977 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 962Water2회HCID 4101HexamethylenetetramineHCID 109994864-(Bromomethyl)-2,2-difluoro-1,3-dioxaindane

생성물 1

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

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f4f080cea95240928f74e252c3352113
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04886816

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