HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471842Generated: October 31, 2026
Nitrogen → 1,1-Dimethylethyl (2-{[4'-(acetylamino)-4-biphenylyl]oxy}ethyl)(4,4-dimethylcyclohexyl)carbamate
https://huagongshe.com/reaction/471842
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Acetamidophenylboronic acid | HCID 2734657 | — |
| Reactant | 1,1-Dimethylethyl {2-[(4-bromophenyl)oxy]ethyl}(4,4-dimethylcyclohexyl)carbamate | HCID 58276240 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1,1-Dimethylethyl (2-{[4'-(acetylamino)-4-biphenylyl]oxy}ethyl)(4,4-dimethylcyclohexyl)carbamate | HCID 58276575 | — |
Reaction Steps
A mixture of 1,1-dimethylethyl {2-[(4-bromophenyl)oxy]ethyl}(4,4-dimethylcyclohexyl)carbamate (0.085 g; 0.20 mmol; Example V-8), [4-(acetylamino)phenyl]boronic acid (0.040 g; 0.22 mmol), PdCl2(dppf).CH2Cl2 (0.005 g; 0.006 mmol), Na2CO3 (2 mL of a 2M solution) and DME (2 mL) was sparged with N2 for 10 minutes at room temperature and heated at 80° for 1 h (until consumption of the aryl bromide, as judged by LC/MS). Upon cooling, the mixture was partitioned between EtOAc/H2O, layers were separated and the aqueous layer was extracted with EtOAc (×2). Combined organics were washed (brine), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc/hexanes), affording the title compound as a pale yellow solid. LC/MS (method A) tR 3.29 min, m/z 481 (M+H, 53%), 381 ([M−Boc]+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633175B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-d8f8417d439c40f6a7439a3c877b86a3 |
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| Source note | uspto-grants-2014_01 |
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