HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534082Generated: October 30, 2026
Dimethylformamide → HCID 67486253, compound
https://huagongshe.com/reaction/534082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [(2S,3S)-1,4-Dioxaspiro[4.5]decane-2,3-diyl]dimethanol | HCID 13128614 | — |
| Product | HCID 67486253 | HCID 67486253 | 45.03% |
Reaction Steps
(2S,3S)-1,4-dioxaspiro[4.5]decane-2,3diyldimethanol (65 g, 321.4 mmol) was dissolved in DMF (500 mL) and cooled in an ice bath. 60% Sodium hydride (15.43 g, 385.7 mmol) was added slowly and the reaction was stirred for 30 minutes in an ice bath then warmed to ambient temperature for 2 hours. Idomethane (20.05 ml, 321.4 mmol) was added and the reaction was stirred at ambient temperature overnight. The majority of the DMF was removed on a rotary evaporator, and the residue was partitioned between aqueous NH4Cl and EtOAc. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified over 1 Kg of SiO2 (20 to 40% EtOAc in hexanes) to afford ((2S,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decane-2-yl)methanol (3.13 g, 144.7 mmol, 45.03% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853409B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-153c3bb007554a86a358f1681dab9028 |
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| Source note | uspto-grants-2014_10 |
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