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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756618Generated: October 28, 2026

2-Morpholinoethanol → HCID 86748393, compound

https://huagongshe.com/reaction/1756618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethanolHCID 61163—
ReactantHCID 9948928HCID 9948928—
SolventTolueneHCID 1140—
ProductHCID 86748393HCID 86748393—

Reaction Conditions

Temperature117 °C

Reaction Steps

7 g (0.02 moles) of (E)-6-(1,3-dihydro-4-amino-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid and toluene (25 ml) are warmed gently to form a solution. A slight excess (1.05 molar equivalents) of 2-morpholinoethanol (3 g, 0.021 moles) and toluene (25 ml) are added. The reaction mixture is stirred for half an hour and then heated to reflux at an initial pot temperature of 117° C. (which increases a few degrees during reflux) under a Dean-Stark trap for 80 hours. The reaction mixture is cooled, washed with water (2×15 ml), 10% aqueous sodium bicarbonate (2×15 ml) and finally with water (15 ml). The toluene layer is stripped to a volume of about 20 ml in vacuo, n-hexane (30 ml) is added and the resulting slurry is aged at room temperature for 2 hours. The product is filtered, washed with n-hexane (ca. 10 ml) and dried in vacuo at 60° C. to yield 2-(morpholin-4-yl)ethyl (E)-6-(1,3-dihydro-4-amino-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441953
Source datasetuspto-grants-1995_08
ORD IDord-8096e783081d48a5bd3c0264ebe76726
Source noteuspto-grants-1995_08