반응 #2664

ord-8ff9fcd9cfe74e8dbd93a16959bf292e

반응 방정식

COc1cc(C=O)cc(C#N)c1O
product
COc1cc(C=O)cc(C#N)c1O
3-formyl-6-hydroxy-5-methoxy benzonitrile
BrB(Br)Br
boron tribromide
N#Cc1cc(C=O)cc(O)c1O
expected product
수율 72.4%
N#Cc1cc(C=O)cc(O)c1O
3-formyl-5,6-dihydroxy benzonitrile
수율 72.4%

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITthe mixture stood for one night at ambient temperature
  2. 2
    농축It was concentrated
  3. 3
    온도cooled again to 0° C.
  4. 4
    workup.ADDITION250 ml of a normal solution of hydrochloric acid were added
  5. 5
    기타The crystallized product was separated out
  6. 6
    세척washed with water
  7. 7
    기타dried
  8. 8
    기타then crystallized from an isopropanol

실험 절차

18 g of the product of Step A and 400 ml of dichloromethane were mixed together under nitrogen and the mixture was cooled to 0° C. 150 ml of a molar solution of boron tribromide in dichloromethane were added and the mixture stood for one night at ambient temperature. It was concentrated, cooled again to 0° C. and 250 ml of a normal solution of hydrochloric acid were added. The crystallized product was separated out, washed with water, dried then crystallized from an isopropanol--water mixture (1-2) to obtain 12 g of the expected product.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05728828uspto-grants-1998_03