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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057336Generated: October 25, 2026

Sodium Methoxide → HCID 178486031, compound

https://huagongshe.com/reaction/2057336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acidHCID 22567682—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178486031HCID 178486031105%

Reaction Steps

5.0 g (16.1 mmol) 5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid in 50 ml methanol were hydrogenated with 0.5 g 10% Pd/C in the presence of 0.94 ml (16.9 mmol, 1.05 eq) sodium methanolate for 1 h at RT. After filtration and evaporation of the solvent, the residue was dissolved in ether and acidified by adding 1M HCl. The organic phase was extracted with water, dried over MgSO4 and evaporated to give 5.3 g (quant) trans-5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexyl]-pentanoic acid as light yellow oil, MS: (312 MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335687B2
Source datasetuspto-grants-2008_02
ORD IDord-a17f48715be64cf5a60ec8e2eec018cf
Source noteuspto-grants-2008_02