HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403990Generated: October 25, 2026
Diethyl chlorophosphate → 2-Tert-butyl-4-methylphenyl diethyl phosphate
https://huagongshe.com/reaction/1403990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | 2-tert-Butyl-4-methylphenol | HCID 17004 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Tert-butyl-4-methylphenyl diethyl phosphate | HCID 59129394 | 100% |
Reaction Steps
To a suspension of NaH (60% in mineral oil, 8.4 g, 0.21 mol) in THF (200 mL) was added dropwise a solution of 2-tert-butyl-4-methylphenol (33 g, 0.20 mol) in THF (100 mL) at 0° C. The mixture was stirred at 0° C. for 15 min and then phosphorochloridic acid diethyl ester (37 g, 0.2.1 mol) was added dropwise at 0° C. After addition, the mixture was stirred at ambient temperature for 30 min. The reaction was quenched with sat. NH4Cl (300 mL) and then extracted with Et2O (350 mL×2). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and then evaporated under vacuum to give 2-tert-butyl-4-methylphenyl diethyl phosphate (contaminated with mineral oil) as a colorless oil (60 g, 100%), which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912199B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-e6d6456a30a64792890f6f5ce5c7b308 |
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| Source note | uspto-grants-2014_12 |
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