HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404398Generated: November 1, 2026
Benzyl Bromide → 8-[2-(Benzyloxy)ethyl]-1,4-dioxaspiro[4.5]decane
https://huagongshe.com/reaction/1404398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1,4-Dioxaspiro(4.5)decan-8-yl)ethan-1-ol | HCID 11805458 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-[2-(Benzyloxy)ethyl]-1,4-dioxaspiro[4.5]decane | HCID 21879603 | 83.2% |
Reaction Steps
To a precooled (0° C.) suspension of NaH (60% in mineral, 0.44 g, 11 mmol) in THF (20 mL) was added 2-(1,4-dioxaspiro[4.5]decan-8-yl)ethanol (1.86 g, 10 mmol) in THF (10 mL). The resulting solution was stirred at 0° C. for 10 min, and allowed to warm to RT, and stirred for 1 h. To the above mixture was added benzyl bromide (1.78 g, 15 mmol) and the resulting mixture was stirred at rt overnight. The reaction was quenched by addition of saturated aqueous NH4Cl solution, extracted with EtOAc, washed with brine, dried over Na2SO4. Purification by flash column chromatography (eluent: 20% EtOAc in hexanes to 30%) gave the product (2.3 g, 83%). LC/MC: 277.1 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912169B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-3411e54154b74f65b7983bd2fe61d6a9 |
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| Source note | uspto-grants-2014_12 |
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