Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Ethyl S-propyl chlorothiophosphate | HCID 11745722 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13343962 | HCID 13343962 | 54% |
Reaction Steps
To a 250 ml round bottom flask equipped with a water condenser, drying tube, magnetic stirrer, and addition funnel was added 4,4'-isopropylidenediphenol (4.57 g, 20 mmol), triethylamine (4.24 g, 42 mmol), and acetonitrile (75 ml). The solution was cooled to 10° C. and O-ethyl S-n-propyl phosphorochloridothioate (8.30 g, 41 mmol) in acetonitrile (25 ml) was added dropwise over 15 minutes. The cooling bath was removed and the reaction warmed to 35° C. for 4 hours. The reaction was diluted with ether (500 ml) and washed successively with water (2×50 ml), 1M NaOH (2×50 ml), 1% HCl (2×50 ml), and brine (2×50 ml). The organic solution was dried (MgSO4) and concentrated under reduced pressure to give the desired product as a colorless oil (6.50 g, 10.8 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04457922 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-befe36765603456192494617e8de10b1 |
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| Source note | uspto-grants-1984_07 |
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