HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Diisopropylamine → Dichloro(diisopropylamino)borane

HRID 842580
Notes
Print preview

Reaction equation

HRID 842580 reaction equation
[Cl:1][B:2]([Cl:4])Cl.[CH:5]([NH:8][CH:9]([CH3:11])[CH3:10])([CH3:7])[CH3:6].C(N(CC)CC)C>C(Cl)Cl>[CH:5]([N:8]([B:2]([Cl:4])[Cl:1])[CH:9]([CH3:11])[CH3:10])([CH3:7])[CH3:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 7912DiisopropylamineHCID 8471TriethylamineHCID 25135Boron Trichloride

Product 1

HCID 4139105Dichloro(diisopropylamino)boraneYield 51%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a methylene chloride solution of trichloroborane (1.0 M, 100 ml, 0.10 mole) was added dropwise at −78° C. diisopropylamine (13.108 ml, 0.100 mole) over a 30 minute period. The solution was allowed to stir for 1 hour, during which a white precipitate formed. The mixture was allowed to warm to room temperature, and solvent was removed under reduced pressure. The residue was dissolved in 100 ml of dry toluene, triethylamine (13.94 ml, 0.10 mole) was added and the solution was stirred overnight at room temperature. The mixture was filtered, the residue was washed with 20 ml of toluene. Solvent was removed under reduced pressure from the combined filtrates, and the resulting oil was purified by vacuum distillation (25-28° C., 13 Pa, 0.1 mm) to give 9.2 g (51 percent) of product as a colorless liquid.

Workup

  1. customformed
  2. customsolvent was removed under reduced pressure
  3. dissolutionThe residue was dissolved in 100 ml of dry toluene
  4. stirringthe solution was stirred overnight at room temperature
  5. filtrationThe mixture was filtered
  6. washthe residue was washed with 20 ml of toluene
  7. customSolvent was removed under reduced pressure from the combined filtrates
  8. distillationthe resulting oil was purified by vacuum distillation (25-28° C., 13 Pa, 0.1 mm)

Sources & evidence

ORD record
ord-b9b7822e9984409395c366ed641c0d1e
Source dataset
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06376406B1

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes