Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169159Generated: November 1, 2026

4-Tert-butyl 1-methyl 2-(benzyloxy)-3-hydroxyfumarate → HCID 178450806, compound

https://huagongshe.com/reaction/2169159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Tert-butyl 1-methyl 2-(benzyloxy)-3-hydroxyfumarateHCID 54679005—
Reactant2-(1-Phenyl-cyclopentyl)-acetamidine HCl saltHCID 86725807—
ReactantHCID 178450818HCID 178450818—
ProductHCID 178450806HCID 17845080651.8%

Reaction Steps

5-Benzyloxy-6-hydroxy-2-(1-phenyl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid tert-butyl ester (27-01) (4.5 g, 51.8%) was synthesized from 2-(1-phenyl-cyclopentyl)-acetamidine HCl salt (26-01) (4.5 g, 18.86 mmol) and (E)-2-benzyloxy-3-hydroxy-but-2-enedioic acid 4-tert-butyl ester 1-methyl ester (4) (10.2 g, 33.41 mmol) as a yellow solid following the procedure as described for 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid tert-butyl ester (6-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-8e6930f80f06466998478e093fdf36cc
Source noteuspto-grants-2015_06