HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864097Generated: October 29, 2026
1-Phenethylamine → HCID 86749880, compound
https://huagongshe.com/reaction/864097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | (2S,3S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxybutanoic acid | HCID 6992538 | — |
| Reactant | Sodium chloride dihydrate | HCID 23713072 | — |
| Reactant | 1-(3-Dimethylaminopropyl)-2-ethylcarbodiimide hydrochloride | HCID 57482816 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86749880 | HCID 86749880 | 93.9% |
Reaction Steps
To a solution of N-Boc-L-allothreonine (0.325 g, 1.48 mmol, 1.00 eq.) and 1-hydroxybenzotriazole hydrate (0.221 g, 1.64 mmol, 1.11 eq.) in dimethylformamide (5 mL) at 0° C. was added 1-(3-dimethylaminopropyl)-2-ethylcarbodiimide hydrochloride (WSC) (0.312 g, 1.63 mmol, 1.10 eq.). After 0.5 hr, a solution of (R) α-methylbenzylamine (0.20 mL, 1.55 mmol, 1.05 eq.) in dimethylformamide (3 mL) was added, followed by 4-methylmorpholine (0.16 mL, 1.46 mmol, 0.98 eq.). After 17 hr, the reaction mixture was poured into a brine/water solution (1:1) and extracted twice with ethyl acetate. The organic layers were combined and washed with aqueous 0.25M potassium hydrogen sulfate, water, aqueous saturated sodium bicarbonate, water, dried over sodium sulfate, and the organic layer concentrated in vacuo to give title compound (0.448 g, 93.9%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561146 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-2e881179245d4df1b236c32befc74f36 |
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| Source note | uspto-grants-1996_10 |
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