HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379964Generated: October 30, 2026
Methyl morpholine oxide → HCID 86750264, compound
https://huagongshe.com/reaction/1379964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 86750265 | HCID 86750265 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86750264 | HCID 86750264 | — |
Reaction Steps
Combine (S)-N-(2-methoxybenzyl)-N-methyl-2-[N'-(t-butoxycarbonyl)-allylamino]-3-(naphth-2-yl)-propionamide (0.46 g, 0.96 mmol), N-methylmorpholine-N-oxide (0.12 g, 1.06 mmol), acetone (20 mL), and water (10 mL). Add osmium tetraoxide (0.50 mL, 0.04M in THF, 0.02 mmol) and stir under an inert atmosphere for 18 hours. Pour the reaction mixture into a saturated solution of sodium bisulfite and extract the intermediate diol into ethyl acetate. Dry the separated organic layer over MgSO4, filter, and evaporate in vacuo to give the crude diol which is taken on to the next step without further purification. Dissolve the crude diol in chloroform (10 mL). Add a solution of lead tetraacetate (0.46 g, 1.06 mmol) in chloroform (10 mL). Stir for 30 minutes and then pour the reaction mixture into a saturated solution of sodium bicarbonate. Extract with dichloromethane and separate the organic layer. Dry the separated organic layer over MgSO4, filter and evaporate in vacuo to give the title compound which may be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05672602 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-7a3b669eb24640518d372f9161f426b3 |
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| Source note | uspto-grants-1997_09 |
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