HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050557Generated: November 1, 2026
4-Methylmorpholine → HCID 20058467, compound
https://huagongshe.com/reaction/2050557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 2-Octylamine | HCID 12735 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 3-Methoxy-α-methyl-4-(phenylmethoxy)benzeneacetic acid | HCID 20058469 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20058467 | HCID 20058467 | — |
Reaction Steps
A solution of 2-(4-benzyloxy-3-methoxyphenyl)propionic acid (5.0 g, 17.5 mmoles) and 4-methylmorpholine (2.0 mL, 17.5 mmoles) in ethyl acetate (170 mL) at 0° C. was treated with isobutyl chloroformate (2.26 mL, 17.5 mmoles). The resulting white slurry was stirred for 20 minutes. A solution of racemic 2-octylamine (2.7 g, 21 mmoles) in ethyl acetate (10 mL total solution) was added to the suspension which was then stirred for 3 hours. The mixture was extracted with 1M hydrochloric acid (3×50 mL), with a saturated sodium bicarbonate solution (3×50 mL), with brine (1×50 mL) and dried over magnesium sulfate. The ethyl acetate was rotary evaporated affording N-2-octyl-2-(4-benzyloxy-3-methoxyphenyl)proprionamide as a white solid which was crystallized from ether/methylene chloride to give 4.55 g. This racemic mixture of diastereomers was separated by silica gel chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013759 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-0fc41069b7164db8b8ae23f64597b449 |
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| Source note | uspto-grants-1991_05 |
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