HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639938Generated: October 30, 2026
Tetrahydrofuran → HCID 86620233, compound
https://huagongshe.com/reaction/639938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Product | HCID 86620233 | HCID 86620233 | — |
Reaction Steps
To a solution a solution of [2-benzyloxy]-5-(4-ethylbenzyl)bromobenzene (5.00 g) in THF (36.5 mL) was added 2.44 M n-butyllithium/n-hexane solution (6.5 mL) at −78° C. and the reaction mixture was stirred for 1 hr at the same temperature. A solution of diethyl chlorophosphate (2.3 mL) in THF (5.6 mL) was added to the reaction mixture at −78° C. and the reaction mixture was stirred for 1 hr at −78° C. The reaction was quenched by the addition of saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane) to give title compound (5.40 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691898B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6daab292a41f4b89bf9bfa5f0e49ba02 |
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| Source note | uspto-grants-2010_04 |
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