HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186661Generated: October 26, 2026
1,2-Dichloroethane → (1S,2S)-2-(7-oxooctanoyl)amino-3-morpholino-1-phenyl-1-propanol
https://huagongshe.com/reaction/2186661
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Oxooctanoic acid | HCID 26464 | — |
| Reactant | (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol | HCID 10513992 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1S,2S)-2-(7-oxooctanoyl)amino-3-morpholino-1-phenyl-1-propanol | HCID 69821324 | 59.1% |
Reaction Steps
A mixed solvent of methylene chloride:methanol=9:1 (20 ml), 7-oxooctanoic acid (700 mg, 4.4 mmol), triethylamine (1.40 ml, 10.0 mmol) and EDC (1.15 g, 6.0 mmol) were added to (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol (944.0 mg, 4.0 mmol), followed by stirring overnight. Methylene chloride (100 ml) was added to the reaction solution. After washed with a saturated sodium hydrogen carbonate solution (50 ml), water (50 ml) and saturated brine (50 ml) successively, the organic layer was dried over sodium sulfate and filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform:ethanol=20:1) to obtain the title compound (890 mg, yield 59%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06407064B2 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-46f28482c5de43128f1566b914bbe8e9 |
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| Source note | uspto-grants-2002_06 |
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