HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62665Generated: October 26, 2026
Potassium Carbonate → tert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamate
https://huagongshe.com/reaction/62665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | tert-Butyl (4-bromo-2-nitrophenyl)carbamate | HCID 52904808 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | tert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamate | HCID 59736984 | 73% |
Reaction Steps
A mixture of tert-butyl (4-bromo-2-nitrophenyl)carbamate (6.0 g, 18.92 mmol, 1.0 eq.), thiophen-2-ylboronic acid (3.2 g, 24.6 mmol, 1.3 eq.), potassium carbonate (7.84 g, 56.8 mmol, 3.0 eq.) and tetrakis(triphenylphosphine)palladium(0) (1.53 g, 1.32 mmol, 0.07 eq.), tri-tolylphosphine in DME/H2O (105 mL) was first degassed then heated to 90° C. for 20 h. The reaction was then filtered through Celite. The product was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by flash column chromatography (silica gel, 2% EtOAc/hexanes) to obtain pure tert-butyl (2-nitro-4-(thiophen-2-yl)phenyl)carbamate (4.42 g, 73% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447030B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-178d9db47d9a475eb399a78fb53ec9fe |
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| Source note | uspto-grants-2016_09 |
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