HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374077Generated: October 25, 2026
Triethylamine → (3-Bromo-2-oxo-piperidin-1-yl)benzoic acid benzyl ester
https://huagongshe.com/reaction/1374077
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl p-aminobenzoate | HCID 98488 | — |
| Reactant | 1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1) | HCID 11012140 | — |
| Reactant | 2,5-Dibromopentanoyl chloride | HCID 11185032 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Bromo-2-oxo-piperidin-1-yl)benzoic acid benzyl ester | HCID 69484348 | — |
Reaction Steps
45.5 g (0.2 mol) of 4-aminobenzoic acid benzyl ester and 30.6 ml (0.22 mol) of triethylamine are dissolved in 200 ml of methylene chloride and added in drops within 45 minutes at 0° C. to a solution of 55.3 g (0.2 mol) of 2,5-dibromovaleric acid chloride (Okawara et al. Chem. Pharm. Bull. (1982), (30), 1225) in 200 ml of methylene chloride, and it is stirred for 18 hours at room temperature. The reaction mixture is now added in drops at 0° C. to a solution of 400 ml of aqueous 32% sodium hydroxide and 2 g of tetrabutylammonium hydrogen carbonate (about 15 minutes), and it is stirred for 30 minutes. Then, the phases are separated, and the aqueous phase is extracted three times with 200 ml of dichloromethane each. The organic phases are dried on sodium sulfate, the solution is evaporated to the dry state and chromatographed on silica gel (methylene chloride). The fractions that contain the product are combined and concentrated by evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07164016B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-c1d6eea1a0cb40208c3684a07952486d |
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| Source note | uspto-grants-2007_01 |
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