HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514810Generated: October 31, 2026
4,4'-Bis(1,1-dimethylethyl)-1,1'-biphenyl → HCID 90419006, compound
https://huagongshe.com/reaction/514810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4'-Bis(1,1-dimethylethyl)-1,1'-biphenyl | HCID 74195 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90419006 | HCID 90419006 | 45.1% |
Reaction Steps
To a suspension of 4,4′-di-tert-butylbiphenyl (DTBB, 30.33 mg, 0.114 mmol) and Li (56.7 mg, 8.09 mmol) in 50 mL of anhydrous THF was added dropwise a solution of (bromomethyl)cyclopropane (307.9 mg, 2.28 mmol) and tert-butyl 4-oxopiperidine-1-carboxylate (500 mg, 2.5 mmol) in anhydrous THF (5 mL) at −78° C. under N2. The resulting mixture was stirred at −78° C. under N2 for 8 h. The reaction mixture was quenched by satd. NH4Cl solution at −78° C. The resulting mixture was extracted with EtOAc (50 mL×2). The combined organic phase was washed with brine, dried over anhy. Na2SO4 and concentrated in vacuo. Column chromatography (15% PE/EtOAc) afforded 262.5 mg of title compound as a colorless oil. 1H NMR (CHLOROFORM-d) δ: 3.90-3.78 (m, 2H), 3.25-3.12 (m, 2H), 1.60 (dd, J=9.4, 4.3 Hz, 4H), 1.48 (s, 9H), 1.42 (d, J=6.9 Hz, 2H), 0.82-0.70 (m, 1H), 0.57-0.47 (m, 2H), 0.16-0.06 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108921B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-2e0fa3fb56624f828c042a378341e6ce |
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| Source note | uspto-grants-2015_08 |
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