Reaction #9178

ord-1345b2679a1f4255af5f660665af3050

Reaction equation

O=C1OCCN1P(=O)(Cl)N1CCOC1=O
bis-(2-oxo-3-oxazolidinyl)-phosphorylchloride
CCN(CC)CC
triethylamine
Cl.NOCc1ccccc1
O-benzylhydroxylamine hydrochloride
O=C(O)CCCCCCCBr
8-bromo octanoic acid
O=C(CCCCCCCBr)NOCc1ccccc1
8-bromo-octanoic acid benzyloxyamide
Yield 78.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGStirring
  2. 2
    ExtractionThe solution was extracted twice with 150 ml each of 1M aqueous hydrochloric acid and twice with 150 ml each of 1M aqueous sodium bicarbonate
  3. 3
    OtherThe organic solvent was removed i

Procedure

In an ice bath, 14 ml triethylamine was added to a suspension of 3.2 g (20 mmol) O-benzylhydroxylamine hydrochloride in 150 ml dichloromethane. Stirring was continued until the solution became clear. Then, 4.5 g (20 mmol) 8-bromo octanoic acid was added, followed by 5.6 g (22 mmol) bis-(2-oxo-3-oxazolidinyl)-phosphorylchloride. Stirring was continued at ambient temperature for 18 h. The solution was extracted twice with 150 ml each of 1M aqueous hydrochloric acid and twice with 150 ml each of 1M aqueous sodium bicarbonate. The organic solvent was removed i. vac. to give 5.1 g (78%) of 8-bromo-octanoic acid benzyloxyamide as a colorless oil. MS: 330 (M+H+)

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091229B2uspto-grants-2006_08