Ethyl Bromide → Triethyl phosphonoacetate

HRID 2384305Notes

Reaction equation

HRID 2384305 reaction equation
[P:1]([O:8][CH2:9][CH3:10])([O:5]CC)[O:2][CH2:3][CH3:4].Br[CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14].BrCC>>[CH2:9]([O:8][P:1]([CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])([O:2][CH2:3][CH3:4])=[O:5])[CH3:10]

Participants

4

Conditions

Temperature
100 °C

Procedure

100 parts by weight of triethyl phosphite and 100 parts by weight of ethyl bromoacetate were put into a reactor equipped with a distillation tube, and the inside of the reactor was substituted by nitrogen. Subsequently, the reactor was heated at 100° C. to start a reaction. Since bromoethane as a by-product began to distill out immediately, the reaction was maintained until the distillation-out of bromoethane slowed down. When the distillation-out of bromoethane became moderate, the reactor was further heated at 150° C. to continue the reaction for 3 hours. The reaction mixture was distilled at 180° C. under a normal pressure to obtain an achromatic transparent liquid (yield of 95%, boiling point of 177° C./760 mmHg).

Workup

  1. customequipped with a distillation tube
  2. customa reaction
  3. distillationto distill out immediately
  4. temperaturethe reaction was maintained until the distillation-out of bromoethane
  5. distillationWhen the distillation-out of bromoethane
  6. temperaturethe reactor was further heated at 150° C.
  7. customthe reaction for 3 hours
  8. distillationThe reaction mixture was distilled at 180° C. under a normal pressure
  9. customto obtain an achromatic transparent liquid (yield of 95%, boiling point of 177° C./760 mmHg)

Sources & evidence

ORD record
ord-efeceadd601d4fc190c11b2cf12226c9
Source dataset
uspto-grants-2012_09
Patent number
US08263690B2

Reaction notes

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