HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516230Generated: October 30, 2026
1,2-Epoxy-3-methoxypropane → HCID 58494657, compound
https://huagongshe.com/reaction/516230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Epoxy-3-methoxypropane | HCID 13589 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | HCID 66982109 | HCID 66982109 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58494657 | HCID 58494657 | — |
Reaction Steps
To a solution of 140 mg of t-butyl 11-ethyl-1,2,3,4,6,7,9,10-octahydro-8H-azepino[4,5-g]quinoline-8-carboxylate in 1.86 ml of acetonitrile was added 0.12 ml of glycidylmethylether, followed by substitution with argon. In an ice-bath, 9 mg of ytterbium(III) trifluoromethanesulfonate was added thereto, followed by stirring at room temperature for 2 hours, then elevating the temperature to 50° C., and stirring overnight. To the reaction mixture were added EtOAc and aqueous sodium bicarbonate, and the organic layer was washed with water and saturated brine. The solvent was evaporated under reduced pressure and the resulting residue was purified by silica gel chromatography (elution solvent: HEX-EtOAc) to obtain 147 mg of t-butyl 11-ethyl-1-(2-hydroxy-3-methoxypropyl)-1,2,3,4,6,7,9,10-octahydro-8H-azepino[4,5-g]quinoline-8-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108977B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a2397d40a49749438dc6a957b43c8190 |
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| Source note | uspto-grants-2015_08 |
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