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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983688Generated: October 31, 2026

Trimethylsilyldiazomethane → HCID 58626990, compound

https://huagongshe.com/reaction/983688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 58626989HCID 58626989—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 58626990HCID 5862699092.4%

Reaction Steps

Trimethylsilyldiazomethane (14 mL of a 2 M solution in hexanes, 26.9 mmol) was added dropwise to a stirring solution of [(1S,3R)-1-carboxymethyl-3-methyl-cyclopentyl]-acetic acid tert-butyl ester (6.9 g, 26.9 mmol) in toluene (60 mL) and methanol (15 mL) at 10° C. under argon, and the mixture was allowed to warm to room temperature. The mixture was stirred for 2 hours, and then the solvent was evaporated under reduced pressure. The residue was taken up in ethyl acetate (200 mL), washed with saturated sodium hydrogen carbonate solution, dilute hydrochloric acid, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by chromatography (silica gel, eluting with a gradient of heptane to 95:5 heptane:ethyl acetate) to give 6.73 g (92.4%) of [(1S,3R)-1-methoxycarbonylmethyl-3-methyl-cyclopentyl]-acetic acid tert-butyl ester;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864390B2
Source datasetuspto-grants-2005_03
ORD IDord-dc07c24beeff44bfb96173a4f84b86a2
Source noteuspto-grants-2005_03