HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547033Generated: October 31, 2026
Ammonium Chloride → HCID 67065139, compound
https://huagongshe.com/reaction/547033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Methyl 2-(4-bromophenyl)acetate | HCID 316783 | — |
| Reactant | HCID 57709132 | HCID 57709132 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67065139 | HCID 67065139 | 46% |
Reaction Steps
N,N-Dimethylformamide (2.0 mL) was added to 2-(4-{1-ethyl-1-[3-methyl-4-(1-trimethylsilanyloxy-cycloheptylethynyl)-phenyl]-propyl}-2-methyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (Example 128-(2); 64.4 mg, 0.110 mmol), (4-bromo-phenyl)-acetic acid methyl ester (30.2 mg, 0.132 mmol), tetrakis(triphenylphosphine)palladium (0) (12.7 mg, 0.0110 mmol) and potassium phosphate (35.0 mg, 0.165 mmol), and the mixture was stirred with microwave heating at 140° C. for seven minutes in a nitrogen atmosphere. An ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=100:0 to 85:15) to give the target compound as a colorless oil (27.0 mg, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935688B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-f33737d2caa74b2ba446b1946606c3d1 |
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| Source note | uspto-grants-2011_05 |
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