Boron tribromide → HCID 178518588, compound

HRID 2255910Notes

Reaction equation

HRID 2255910 reaction equation
[CH2:1]([C:8]1[C:9](=[O:22])[C:10]2[CH:21]=[CH:20][CH:19]=[CH:18][C:11]=2[NH:12][C:13](=[O:17])[C:14]=1[O:15]C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.B(Br)(Br)Br>ClCCl>[CH2:1]([C:8]1[C:9](=[O:22])[C:10]2[CH:21]=[CH:20][CH:19]=[CH:18][C:11]=2[NH:12][C:13](=[O:17])[C:14]=1[OH:15])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 25134Boron tribromideHCID 19704908HCID 19704908, compound

Product 1

HCID 178518588HCID 178518588, compoundYield 78.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 4-benzyl-3-methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine (0.45 g) in dichloromethane was added boron tribromide (4.6 mL). Upon completion of the reaction, the mixture was added to ice water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried and evaporated. The resulting solid was recrystallized from toluene to give the title compound (0.336 g); mp 199°-200° C.; NMR: 3.97 (s,2); MS(EI): m/z=279(M). Analysis for C17H13NO3.0.1 H2O: Calculated: C, 72.64; H, 4.73; N, 4.98; Found: C, 72.65; H, 4.59; N, 4.94.

Workup

  1. customUpon completion of the reaction
  2. extractionextracted with ethyl acetate
  3. washThe combined organic extracts were washed with brine
  4. customdried
  5. customevaporated
  6. customThe resulting solid was recrystallized from toluene

Sources & evidence

ORD record
ord-429d8f84d7fb4a2bb70c59867be02159
Source dataset
uspto-grants-1997_08
Patent number
US05654295

Reaction notes

Loading…