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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985123Generated: October 30, 2026

HCID 57718998, compound → HCID 10195632, compound

https://huagongshe.com/reaction/1985123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57718998HCID 57718998—
SolventMethanolHCID 887—
ProductHCID 10195632HCID 1019563298%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(4-{3-[1-(4-tert-Butyl-benzyl)-3-methyl-2-oxo-imidazolidin-4-yl]-propyl}-2-methyl-phenoxy)-2-methyl-propionic acid ethyl ester (0.065 g, 0.128 mmole) is treated with 3:1 MeOH/5.0N NaOH (4 mL) at room temperature overnight, and then concentrated. The resulting residue is diluted with water (2 mL), cooled down to 0° C., acidified to pH=2 by adding concentrated HCl dropwise. The aqueous suspension is loaded on a Chem elut tube and eluted with DCM (50 mL). Evaporation of methylene chloride gives the titled compound as an oil (0.060 g, 98%). Mass [EI+] 481 (M+H)+, [EI−] 479 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544812B2
Source datasetuspto-grants-2009_06
ORD IDord-16bc7c04ce9b40a4821aa1cb8ecb75d0
Source noteuspto-grants-2009_06