HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451857Generated: October 31, 2026
Ammonium Hydroxide → HCID 69601970, compound
https://huagongshe.com/reaction/1451857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 15435489 | HCID 15435489 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69601970 | HCID 69601970 | 23.3% |
Reaction Steps
A mixture of 3-(cis-hexahydrophthalimido)-3-phenylpropionic acid (0.903 g, 3.00 mmol) and carbonyldiimidazole (0.525 g, 3.75 mmol) in 13 mL of anhydrous tetrahydrofuran under nitrogen was stirred for 1 hour, then 0.25 mL of concentrated ammonium hydroxide was added to the reaction solution. After 20 minutes, the reaction mixture was concentrated in vacuo to an oil. The oil was diluted with 20 mL of water and the mixture extracted with ethyl acetate (20 mL). The organic layer was dried (sodium sulfate) and concentrated to afford an oil. The oil was then purified by flash chromatography (silica gel, 5/95 methanol/methylene chloride, Rf =0.3) to afford 210 mg of 3-(cis-hexahydrophthalimido)-3-phenylpropionamide as an oil which slowly crystallized to an ivory solid: 1H NMR (DMSO-d6) δ7.49 (s, 1 H, NH), 7.4-7.2 (m, 5 H, Ar), 6.90 (s, 1 H, NH), 5.54 (t, 1 H, J=7.8 Hz, CH), 3.09 (d, 2 H, J=7.8 Hz, CH2), 2.95-2.80 (m, 2 H, CH2), 1.8-1.1 (m, 8 H); 13C NMR (DMSO-d6) δ 179.6, 179.5, 171.5, 139.5, 128.6, 127.7, 127.2, 55.2, 50.6, 38.8, 36.5, 23.4, 23.3,21.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605914 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-6835d5e0fcd4427a9e7e931994a8fb67 |
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| Source note | uspto-grants-1997_02 |
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