Benzene → HCID 12906828, compound

HRID 225226

Reaction equation

HRID 225226 reaction equation
C1C=CC=CC=1.[CH3:7][C:8]1([CH3:14])[NH:12][CH2:11][CH:10]([CH3:13])[O:9]1.C(N(CC)CC)C.[Br:22][CH:23]([CH2:27][Br:28])[C:24](Cl)=[O:25]>O>[CH3:7][C:8]1([CH3:14])[N:12]([C:24](=[O:25])[CH:23]([Br:22])[CH2:27][Br:28])[CH2:11][CH:10]([CH3:13])[O:9]1

Participants

6

Reactant 4

HCID 241Benzene2×HCID 8471TriethylamineHCID 867902,3-Dibromopropanoyl chlorideHCID 95486Oxazolidine, 2,2,5-trimethyl-

Product 1

HCID 12906828HCID 12906828, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Fourteen (14 ml.) milliliters of a benzene solution containing 3.5 g. of 2,2,5-trimethyl oxazolidine was added to 25 ml. of benzene and 3.5 g. of triethylamine. Seven and one-half (7.5 g.) grams of 2,3-dibromopropionyl chloride was added dropwise with stirring and cooling in an ice bath. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over anhydrous magnesium sulfate and the solvent stripped under vacuum. The yield was 5.7 g. of an oil, nD30 =1.5060.

Workup

  1. temperaturecooling in an ice bath
  2. customWhen reaction
  3. customthe benzene layer separated
  4. dry with materialdried over anhydrous magnesium sulfate

Sources & evidence

ORD record
ord-95a628796b614d20b2674ec6f8d6eea6
Source dataset
uspto-grants-1980_11
Patent number
US04236011

Linked notes

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