Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Product | Triethyl phosphonoacetate | HCID 13345 | 95% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263690B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-efeceadd601d4fc190c11b2cf12226c9 |
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| Source note | uspto-grants-2012_09 |
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