HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488187Generated: October 28, 2026
Benzyl Bromide → Tert.butyl(benzyl)(diethoxymethyl)phosphine oxide
https://huagongshe.com/reaction/488187
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178472281 | HCID 178472281 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert.butyl(benzyl)(diethoxymethyl)phosphine oxide | HCID 19938721 | — |
Reaction Steps
Tertiary-butyl(diethoxymethyl)phosphine oxide (2.5 g), (0.012 mol) is dissolved in 35 ml of dry tetrahydrofuran and cooled to -78° C. under an argon atmosphere. To this stirred solution is added 9.0 ml of n-butyl lithium (1.6M solution in hexane) and the mixture is stirred at -78° C. for 10 minutes. After this time, a solution of 2.47 g (0.014 mol) of benzyl bromide in 15 ml of dry tetrahydrofuran is added, and the reaction mixture is allowed to warm to room temperature. After stirring for 3 hours at room temperature, 10 ml of saturated ammonium chloride solution is added and the product is extracted into diethyl ether (2×100 ml). The combined organic extracts are dried and evaporated under reduced pressure to give a crude product. This is purified by chromatography on silica, using ethyl acetate as eluent, to give tertiary-butyl(benzyl)(diethoxymethyl) phosphine oxide as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298663 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-406c02746e264f69946b10ae83462c92 |
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| Source note | uspto-grants-1994_03 |
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