Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 4-((6-Bromohexyl)oxy)-3-chloroanisole | HCID 92068 | — |
| Product | Fosarilate | HCID 71756 | 79.2% |
Reaction Steps
Triethyl phosphite (185 g, 230 ml, 1.1 mole) was placed in a flask equipped with a thermometer, dropping funnel, stirrer and 8 inch Vigreux column with condenser set for downward distillation. The phosphite was heated to 158° C. thereby inducing mild reflux. 6-(2-Chloro-4-methoxyphenoxy)hexyl bromide (320 g, 1 mole) was then added dropwise over a period of 50 minutes. The reaction mixture was heated for an additional 90 minutes at which time distillation of ethyl bromide ceased. The remaining reaction mixture was distilled in vacuo and the fraction (250 g) boiling at 183°-197° C. (0.2-0.3 mm) was collected. The latter was combined with 79 g of product obtained from another run starting from 100 g of bromide and redistilled to give 300 g of diethyl [6-(2-chloro-4-methoxyphenoxy)-hexyl]phosphonate, b.p. 202°-204° C. (0.02 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182759 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-2a3e2a9b117147dbb705b7b97912f062 |
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| Source note | uspto-grants-1980_01 |
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