HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011653Generated: October 31, 2026
Formaldehyde → 4-(4-Bromo-2-fluoro-phenyl)-1-methyl-pyrrolidine-3-carboxylic acid (4-chloro-phenyl)-amide
https://huagongshe.com/reaction/1011653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sarcosine | HCID 1088 | — |
| Reactant | 3-(4-Bromo-2-fluoro-phenyl)-N-(4-chloro-phenyl)-acrylamide | HCID 67313812 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(4-Bromo-2-fluoro-phenyl)-1-methyl-pyrrolidine-3-carboxylic acid (4-chloro-phenyl)-amide | HCID 59454160 | 40% |
Reaction Steps
A mixture of paraformaldehyde (15.3 g, 0.51 mol) and 3-(4-bromo-2-fluoro-phenyl)-N-(4-chloro-phenyl)-acrylamide (15 g, 42.5 mmol) was heated under reflux in toluene (150 mL), and sarcosine (15.2 g, 170 mmol, 4.0 equiv) was added in 4 portions over 4 hrs, the H2O formed was removed with the aid of a Dean-Stark trap. After 4 hours, the cooled mixture was filtered. The filtrate was concentrated, and the residue was purified by chromatography on silica gel eluted with dichloromethane-methanol to give 7.0 g of 4-(4-bromo-2-fluoro-phenyl)-1-methyl-pyrrolidine-3-carboxylic acid (4-chloro-phenyl)-amide. Yield was 40%. MS: calc'd 411 (MH+), exp 411 (MH+). 1H NMR (CDCl3, 400 MHz), 9.71 (s, 1H), 7.57 (d, 2H, J=8.8 Hz), 7.51 (t, 1H, J=7.6 Hz), 7.24 (t, 4H, J=8.8 Hz), 4.30 (q, 1H, J=8.8 Hz), 3.76-3.94 (m, 2H), 3.40-3.62 (m, 3H), 2.92 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977372B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-d486ca5d518a447cb6e79ac04046c5fc |
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| Source note | uspto-grants-2011_07 |
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