تفاعل #45450

ord-282782dd16794bb7bdd7cd11cc6d17f7

معادلة التفاعل

O=C([O-])O.[Na+]
sodium bicarbonate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrC(Br)(Br)Br
carbon tetrabromide
CC(C)(C)OC(=O)N1CCCC1C=O
2-formyl -pyrrolidine-1-carboxylic acid tert-butyl ester
CC(C)(C)OC(=O)N1CCC[C@H]1C=C(Br)Br
desired product
المردود 86.0%
CC(C)(C)OC(=O)N1CCC[C@H]1C=C(Br)Br
tert-butyl (2S)-2-(2,2-dibromovinyl)pyrrolidine-1-carboxylate
المردود 86.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىseparated
  2. 2
    تجفيفThe organic phase was dried (MgSO4)
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe concentrate was purified by flash chromatography on silica gel using 0-1% methanol/dichloromethane

الإجراء التجريبي

A solution of triphenylphosphine (21.1 g, 80.3 mmol) and carbon tetrabromide (13.32 g, 40.16 mmol) in dichloromethane (300 mL) at 0° C. was treated with a solution of 2-formyl -pyrrolidine-1-carboxylic acid tert-butyl ester (4.0 g, 20.08 mmol) in dichloromethane (10 mL) dropwise via syringe. The solution was stirred for 1 hour at room temperature, poured into a saturated sodium bicarbonate solution and separated. The organic phase was dried (MgSO4), filtered and concentrated. The concentrate was purified by flash chromatography on silica gel using 0-1% methanol/dichloromethane to give 6.13 g (86% yield) of the desired product. 1H NMR (300 MHz, CHLOROFORM-D) δ ppm 1.47 (s, 9H), 1.81 (m, 3H), 2.16 (m, 1H), 3.39 (m, 2H), 4.37 (s, 1H), 6.38 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737160B2uspto-grants-2010_06