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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654545Generated: October 29, 2026

Triethylamine → Trans-(E)-6-{2-{2-(4-fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6,6-dimethylcyclohex-1-en-1-yl}ethenyl}-4-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

https://huagongshe.com/reaction/654545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl (E)-7-{2-(4-fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6,6-dimethylcyclohex-1-en-1-yl}-3,5-dihydroxyhept-6-enoateHCID 86744089—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductTrans-(E)-6-{2-{2-(4-fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6,6-dimethylcyclohex-1-en-1-yl}ethenyl}-4-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-oneHCID 86744090—

Reaction Steps

In a manner similar to Scheme I, 34 (0.19 g) was treated with 2N NaOH in methanol at 0°-5° C. for 18 h, followed by ethyl chloroformate (0.254 mmol) and Et3N in CH2Cl2 at 0°-5° C. Workup and purification of the residue by SiO2 using 1% Et3N in EtOAc as eluent yielded the product. mp 120°-3° C. Anal. C26H34FNO3 ·0.5 H2O: Theory C: 71,53; H: 8.08; N: 3.21; Found C: 71.60; H: 8.17; N: 3.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132312
Source datasetuspto-grants-1992_07
ORD IDord-1ac5941a8e984036981e7ce47705a9a0
Source noteuspto-grants-1992_07