HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767094Generated: November 1, 2026
HCID 54248964, compound → HCID 54031485, compound
https://huagongshe.com/reaction/1767094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 54248964 | HCID 54248964 | — |
| Reactant | Trimethylsilyldiazomethane hexane | HCID 86587183 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54031485 | HCID 54031485 | — |
Reaction Steps
50 cm3 of a solution of 2M trimethylsilyldiazomethane/hexane are added, at a temperature in the region of 15° C., under an argon atmosphere, to 5 g (17.64 mmol) of (3R,4R)-1-tert-butyloxycarbonyl-4-(2-carboxyethyl)-3-vinylpiperidine in solution in 50 cm3 of methanol. After stirring for 3 hours at a temperature in the region of 22° C., the reaction medium is concentrated to dryness under reduced pressure (2.7 kPa) to give 5.3 g of (3R,4R)-1-tert-butyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-vinylpiperidine in the form of an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07232834B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-7705154a249748f68bfb118ed69a7bfc |
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| Source note | uspto-grants-2007_06 |
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