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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767094Generated: November 1, 2026

HCID 54248964, compound → HCID 54031485, compound

https://huagongshe.com/reaction/1767094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54248964HCID 54248964—
ReactantTrimethylsilyldiazomethane hexaneHCID 86587183—
SolventMethanolHCID 887—
ProductHCID 54031485HCID 54031485—

Reaction Conditions

Temperature22 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232834B2
Source datasetuspto-grants-2007_06
ORD IDord-7705154a249748f68bfb118ed69a7bfc
Source noteuspto-grants-2007_06