HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987917Generated: October 30, 2026
Sodium Bicarbonate → HCID 69855343, compound
https://huagongshe.com/reaction/987917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 86759213 | HCID 86759213 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69855343 | HCID 69855343 | 45.7% |
Reaction Steps
A solution of 4-benzyl-5-(2-formyl-3-methoxycarbonyl-5-oxo-hexyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (13.5 g, 27 mmol) and para-toluenesulfonic acid monohydrate (660 mg, 2.7 mmol) in dry toluene (250 ml), was refluxed for 24 hours using a Dean-Stark apparatus to remove water formed during the reaction. The mixture was then cooled to room temperature and treated with and saturated aqueous sodium hydrogen carbonate solution (20 ml). After dilution with ethyl acetate and brine, the layers were separated and the aqueous layer extracted with ethyl acetate. The combined organic layers were washed with brine, dried (anhydrous magnesium sulfate) and concentrated in vacuo. Purification by flash chromatography on silica gel provided 4-benzyl-5-(6-methoxycarbonyl-4-oxo-cyclohex-2-enylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (5.64 g, 43%). Mass spectrum 458 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632826B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-0caed817204d47319725e428b1d15f83 |
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| Source note | uspto-grants-2003_10 |
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