HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260119Generated: November 1, 2026
2-Morpholinoethanol → HCID 86749565, compound
https://huagongshe.com/reaction/260119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | HCID 9797036 | HCID 9797036 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86749565 | HCID 86749565 | — |
Reaction Steps
7 g of (E)-6-(4-amino-1,3-dihydro-6-ethyl-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 of 2-morpholinoethanol (3 g) 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 -(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05525602 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-1ff720306b70421284d8fafc19397995 |
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| Source note | uspto-grants-1996_06 |
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