HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458788Generated: October 30, 2026
Ethyl chloroformate → 3-(4-Benzyloxy-3-methoxy-phenyl)-propionamide
https://huagongshe.com/reaction/458788
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(3-Methoxy-4-benzyloxyphenyl)propionic acid | HCID 2752415 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Benzyloxy-3-methoxy-phenyl)-propionamide | HCID 18442581 | 100% |
Reaction Steps
To a stirred solution of 3-(4-benzyloxy-3-methoxy-phenyl)-propionic acid (8.38 g, 29.30 mmol) in dry THF (110 ml), under nitrogen, was added TEA (4.5 ml, 32.33 mmol), and the resulting mixture was cooled to −10° C. before ethyl chloroformate (3.1 ml, 32.53 mmol) was added dropwise. After stirring at −10° C. (20 min), ammonium hydroxide (25% in water, 65 ml) in THF (65 ml) was added and the mixture was stirred at −15° C. for 30 min and then at RT for 1.5 h. The reaction mixture was concentrated in vacuo, extracted three times with CH2Cl2 and the combined organic extracts were washed with saturated aqueous NaHCO3 and brine. The organic phase was dried over anhydrous MgSO4, filtered and concentrated to give the title compound (8.40 g, 29.30 mmol, 100%) as a colorless solid. No further purification of the crude amide was necessary.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192950B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-4b87c93c90e7498ea6fef75bd7789d22 |
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| Source note | uspto-grants-2007_03 |
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