HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600293Generated: October 29, 2026
Potassium Carbonate → (S)-tert-butyl 1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamate
https://huagongshe.com/reaction/600293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Cyanophenylboronic acid | HCID 2734325 | — |
| Reactant | (S)-Tert-butyl (1-cyano-2-(4-iodophenyl)ethyl)carbamate | HCID 57999650 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | (S)-tert-butyl 1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamate | HCID 57999672 | 90.2% |
Reaction Steps
A solution of 3-cyanophenylboronic acid (4.74 g), (S)-tert-butyl 1-cyano-2-(4-iodophenyl)ethylcarbamate (10 g) and bis[bis(1,2-diphenylphosphino)-ethane]palladium (0) (0.243 g) in dioxane (100 mL) under nitrogen, was stirred for 10 min. A solution of potassium carbonate (7.43 g) in water (30 mL) was added and the resulting solution was stirred at 75° C. for 3 h. The cooled mixture was poured into water containing brine and extracted with ethyl acetate (3×150 mL). The combined organics were washed with saturated brine (3×50 mL), dried over sodium sulfate and adsorbed onto silica. The crude product was purified by flash silica chromatography, eluting with 20% ethyl acetate in isohexane. Pure fractions were evaporated to dryness to afford (S)-tert-butyl 1-cyano-2-(3′-cyanobiphenyl-4-yl)ethylcarbamate (8.42 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902181B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-5e2ea4f11b1a492c822d78036c4699b7 |
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| Source note | uspto-grants-2011_03 |
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