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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4504Generated: October 26, 2026

Dicyclohexylcarbodiimide → morpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate

https://huagongshe.com/reaction/4504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-MorpholinoethanolHCID 61163—
ReactantE-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acidHCID 67854275—
SolventTetrahydrofuranHCID 8028—
Productmorpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoateHCID 67854272—

Reaction Steps

To 1.0 g of E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acid dissolved in 20 ml of dry THF is added 0.59 g of dicyclohexylcarbodiimide and 0.037 g of N-(2-hydroxyethyl)morpholine. The mixture is left at room temperature for 6 hours, then evaporated to dryness. The residue is chromatographed on silica gel, eluting with 50:1 dichloromethane:methanol, to give morpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727069
Source datasetuspto-grants-1988_02
ORD IDord-8099b77f8ff84220a75161afb1f5b51b
Source noteuspto-grants-1988_02