HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228862Generated: October 30, 2026
Sodium Bicarbonate → (S)-oxiranylmethyl-carbamic acid benzyl ester
https://huagongshe.com/reaction/2228862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | benzyl N-[(2S)-2,3-dihydroxypropyl]carbamate | HCID 11310670 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (S)-oxiranylmethyl-carbamic acid benzyl ester | HCID 10375722 | 90% |
Reaction Steps
(S)-2,3-Dihydroxy-1-propylcarbamate benzyl ester (2.11 g, 0.01 mol) in 100 ml flask was dissolved in CHCl3 (30 ml). 1-Chlorocarbonyl-1-methylethylacetate (1.8 ml, 0.013 mol) was added and stirred for 3 hours at ambient temperature. Sat. aqueous solution of NaHCO3 (20 ml) was added and extracted three times with ethyl acetate (50 ml). The organic layer was evaporated and dissolved in THF (50 ml). Sodium methoxide (0.53 g, 0.01 mol) was added and stirred for 6 hours. Sat. aqueous solution of NaHCO3 (50 ml) was added and extracted with ethyl acetate (50 ml). The organic layer was dried over anhydrous MgSO4 and evaporated to dryness. The crude product was purified by column chromatography on silica gel to give (S)-2,3-epoxy-1-propylcarbamate benzyl ester (90%, optical purity>99%ee).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417403B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-7fce327d3be8414bab7091212ab0b61d |
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| Source note | uspto-grants-2002_07 |
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