HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227455Generated: October 30, 2026
3,4-Dichlorobenzoic acid → tert-Butyl[(2S)-4-(3,4-dichlorobenzoyl)morpholin-2-yl]methylcarbamate
https://huagongshe.com/reaction/227455
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dichlorobenzoic acid | HCID 5817 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (R)-2-N-Boc-aminomethylmorpholine | HCID 42556135 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl[(2S)-4-(3,4-dichlorobenzoyl)morpholin-2-yl]methylcarbamate | HCID 86760232 | 86% |
Reaction Steps
A mixture of 3,4-dichlorobenzoic acid (0.5 g), 1-hydroxybenzotriazole (0.376 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.432 g), and N,N-diisopropylethylamine (0.485 ml) in N,N-dimethylformamide (10 ml) was stirred at 20° C. for 10 min. The mixture was treated with tert-butyl(2R)-morpholin-2-ylmethylcarbamate (0.500 g, known compound WO 9639407A1) and stirred at 20° C. for 24 h. The mixture was partitioned between ethyl acetate (75 ml) and 2N aqueous hydrochloric acid (50 ml). The phases were separated and the organic extract washed with 2N aqueous hydrochloric acid (50 ml), saturated aqueous sodium hydrogen carbonate (2×50 ml), dried (MgSO4) and filtered. The solvent was removed in vacuo to give the title compound as a yellow oil, (0.774 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560548B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-ee2163203b874d4c80efef4541125669 |
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| Source note | uspto-grants-2009_07 |
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