HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964557Generated: October 26, 2026
1,2-Dichloroethane → Boc-Phe Morpholinamide
https://huagongshe.com/reaction/964557
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Boc-Phe morpholine | HCID 131720327 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Boc-Phe Morpholinamide | HCID 131717846 | 99% |
Reaction Steps
A 250 ml flask was charged with Boc-Phe-OH (10 g, 38 mmol), morpholine (3.3 g, 38 mmol) and 1-hydroxybenztriazole (5.1 g, 38 mmol) in 100 ml dry dimethylformamide (DMF). To this solution was added diisopropylethylamine (DIEA) at zero degrees C until the pH value reached 8, followed by addition of EDC (8.8 g, 46 mmol). The solution was slowly warmed to room temperature. The mixture was stirred for eight hours at room temperature (about 22° C.). The DMF was removed by vacuum evaporator, ethyl acetate and water were added, and the layers were separated. The aqueous layer was extracted with ethyl acetate (50 ml×2), combined extracts were washed with 1N HCl, saturated NaHCO3, water and brine, dried with MgSO4, filtered and concentrated to give a colorless liquid (12.8 g, 37.7 mmol; 99 percent yield) that was characterized by 1 HNMR as Boc-Phe-morpholine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05770573 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-7c63985e2a6144ae81028e3a61d86372 |
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| Source note | uspto-grants-1998_06 |
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