HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488167Generated: October 27, 2026
Sodium Bicarbonate → HCID 15235904, compound
https://huagongshe.com/reaction/488167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Farnesyl bromide | HCID 550199 | — |
| Reactant | Diethyl (t-Butyldimethylsiloxy)methylphosphonate | HCID 12606850 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15235904 | HCID 15235904 | — |
Reaction Steps
To a stirred solution of the diethyl (t-butyldimethylsiloxy)methylphosphonate (562 mg, 2.0 mmol) in THF (5 ml) under argon at -78° C. was added n-BuLi (0.84 ml of a 2.5M solution in hexanes, 2.1 mmol) and the resulting mixture stirred at -78° C. for 15 min. Farnesyl bromide (0.542 ml, 2.0 mmol) was added to the mixture over 5 min and the solution stirred a further 1 hr at -78° C. and then allowed to warm to r.t. The reaction mixture was poured into saturated NaHCO3 solution and the organic solvent evaporated in vacuo, the residue was extracted into ethylacetate and washed with brine, dried (MgSO4) and concentrated in vacuo and the resulting oil chromatographed on silica gel eluted with ethylacetate:hexanes (3:7, v:v). to afford the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298655 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-6fdc9fcdf24347d085bd383cf6b651ef |
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| Source note | uspto-grants-1994_03 |
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