HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640500Generated: October 26, 2026
Cesium carbonate → (R)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-5-hydroxymethyl-oxazolidin-2-one
https://huagongshe.com/reaction/1640500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (2R)-Oxiran-2-ylmethyl butanoate | HCID 2724536 | — |
| Reactant | (2,3-Dihydro-benzo[1,4]dioxin-6-yl)-carbamic acid benzyl ester | HCID 66736198 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-5-hydroxymethyl-oxazolidin-2-one | HCID 66737186 | 41% |
Reaction Steps
A solution of (2,3-dihydro-benzo[1,4]dioxin-6-yl)-carbamic acid benzyl ester (3.0 g, 10.5 mmol, prepared according to method C) in THF (60 mL) was cooled to −78° C. before the dropwise addition of n-BuLi (5.1 mL of a 2.5M solution in hexanes, 1.2 eq.). The mixture was stirred at −78° C. for 1 h and then warmed to −15° C. At this temperature (R)-glycidyl butyrate (1.98 g, 1.2 eq.) was added dropwise. The mixture was stirred at rt overnight. Cs2CO3 (tip of a spatula) was added and the mixture heated at 40° C. until complete conversion. The mixture was diluted with EA and washed with sat. NH4Cl solution and water. The org. layer was dried over MgSO4 and concentrated. Chromatography on SiO2 (Hex/EA 2:1, 1:1) gave the desired intermediate as a beige solid (1.09 g, 41% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114867B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-bc68aebb50bf4bed88638f92f0be2ae9 |
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| Source note | uspto-grants-2012_02 |
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