HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889697Generated: November 1, 2026
Diisopropylethylamine → HCID 57665994, compound
https://huagongshe.com/reaction/889697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Reactant | HCID 57665930 | HCID 57665930 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | HCID 57665994 | HCID 57665994 | 50% |
Reaction Steps
4-Methyl-2-[4′-trifluoromethyl-5-(6-trifluoromethyl-piperidin-2-yl)-biphenyl-3-yl]-pentanoic acid ethyl ester 7b (37 mg, 0.072 mmol), 4-trifluoromethylbenzyl bromide (86 mg, 0.36 mmol), DIEA (125 μl, 0.72), and tetrabutylammonium iodide (TBAI)(10 mg, 0.096 mmol) were combined and heated under microwave conditions to 150° C. After several additions of the starting materials and ˜90 minutes under microwave, ˜50% product was formed. The reaction was diluted with EtOAc, washed with brine, sat. NaHCO3, and brine, dried over magnesium sulfate and filtered. Purification by silica gel chromatography gave the product as yellow oil. (25 mg, 52%) (M+H) 73.65, Found 674.4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08252935B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-a90243b17b534e34b8cba9d89a68b835 |
|---|
| Source note | uspto-grants-2012_08 |
|---|