HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448899Generated: October 30, 2026
Potassium Carbonate → 4-[4-Bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl ester
https://huagongshe.com/reaction/448899
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 4-bromobutanoate | HCID 2757253 | — |
| Reactant | 5-bromo-4-chloro-2-hydroxy-N-methyl-N-o-tolyl-benzamide | HCID 68602612 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[4-Bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl ester | HCID 68602722 | 82.7% |
Reaction Steps
To 5-bromo-4-chloro-2-hydroxy-N-methyl-N-o-tolyl-benzamide (2.6 g, 7.3 mmol) in dry DMF (30 mL), was added K2CO3 (2.0 g, 7.6 mmol), followed by addition of t-butyl 4-bromobutyrate (2.0 g, 8.8 mmol). The mixture was heated at 60° C. for 12 hrs and partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, and dried over MgSO4. After filtration, concentration and purification by silica gel column chromatography eluting with ethyl acetate in hexanes (3/7) gave 4-[4-bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl ester (3.0 g). MS: 496.3 (M+H)+; tR=2.81 min (method 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481738B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-dc84627a5d9744a19f56779605063ebe |
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| Source note | uspto-grants-2013_07 |
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