Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | (3R,4S)-3,4-dihydroxydihydrofuran-2(3H)-one | HCID 2724794 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13388560 | HCID 13388560 | — |
Reaction Steps
A solution of 5.50 g (46.57 mmoles) L-threonolactone in 100 mL MeOH, previously saturated with anhydrous NH3 at 0° C., was kept at room temperature for 48 h in a pressure bottle. The solvent was evaporated in vacuo, the residual oil re-evaporated from absolute EtOH, and the resulting solid crystallized from boiling EtOH. The crystals were collected after cooling at 0° C., washed with EtOH-Et2O (1:1 parts by volume), then with Et2O, and dried at 40° C./0.005 mm Hg to give 6.023 g (95.7%) of analytically pure product L-threonamide, m.p. 105°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663469 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-53d8b9a0d56d4064bd3e00364ed5dd3a |
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| Source note | uspto-grants-1987_05 |
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