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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 932217Generated: November 2, 2026

Trimethylsilyldiazomethane → HCID 67999455, compound

https://huagongshe.com/reaction/932217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 67999791HCID 67999791—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
ProductHCID 67999455HCID 67999455—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-((3R,5R,6S)-1-((S)-2-(tert-butyldiphenylsilyloxy)-1-cyclopropylethyl)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-3-yl)acetic acid (1400 mg, 1.96 mmol; Example 263, Step A) in a mixture of MeOH (3.1 mL) and benzene (12.5 mL) was added 2.0 M (trimethylsilyl)diazomethane in hexanes (1.96 mL, 3.92 mmol) at 0° C. dropwise. After being stirred at 0° C. for 1 h, the reaction was concentrated under reduced pressure. Purification of the residue by chromatography on silica gel (40 g SiO2, 10%, and 20% EtOAc/Hex) provided the title compound as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296736B2
Source datasetuspto-grants-2016_03
ORD IDord-75b42b5fddab4c8ab669a301c1833f1c
Source noteuspto-grants-2016_03