HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366347Generated: October 27, 2026
1,2-Dichloroethane → (2S)-2-[(benzyloxy)methyl]-1,4-dioxane
https://huagongshe.com/reaction/1366347
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (R)-3-(benzyloxy)propane-1,2-diol | HCID 2724795 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2S)-2-[(benzyloxy)methyl]-1,4-dioxane | HCID 66971993 | — |
Reaction Steps
(2R)-3-(benzyloxy)propane-1,2-diol (2.00 g, 11.0 mmol) and tetrabutylammonium bromide (708 mg, 2.20 mmol) were dissolved in 50 mL of 1,2-dichloroethane, then 50 mL of a 50% (w/w) aqueous sodium hydroxide solution was added quickly and the mixture was heated to 50° C. After 18 h, an additional 50 mL of 1,2-dichloroethane and 50 mL of 50% (w/w) sodium hydroxide solution was added. After 8 h, additional 50 mL of 1,2-dichloroethane was added. After 72 h, the mixture was diluted in diethyl ether, washed with water and brine, then dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (silica, ethylacetate/hexanes) to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 7.26-7.35 (m, 5H); 4.51-4.56 (m, 2H); 3.72-3.82 (m, 4H); 3.67-3.71 (m, 1H); 3.58-3.64 (m, 1H); 3.38-3.48 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893081B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-aa37bea96fbe49a3bfeece8564a61d37 |
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| Source note | uspto-grants-2011_02 |
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