HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897947Generated: October 29, 2026
Triethylamine → N2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amine
https://huagongshe.com/reaction/897947
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Bromophenyl isothiocyanate | HCID 16133 | — |
| Reactant | 2-Amino-6-isopropylphenol | HCID 14684982 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amine | HCID 22347135 | 91% |
Reaction Steps
A solution of 2-amino-6-isopropylphenol (0.354 g, 2.34 mmol) and 4-bromophenylisothiocyanate (0.500 g, 2.34 mmol) in tetrahydrofuran (35 mL) was stirred at room temperature for 3 h. Anhydrous copper (II) sulfate (3.361 g, 21.06 mmol), silica gel (3.361 g), and triethylamine (0.236 g, 0.33 mL, 2.34 mmol) were added, and the mixture stirred at room temperature for 18 h. The reaction mixture was filtered through a pad of Celite and the washed with diethyl ether (3×50 mL). The filtrate was concentrated to afford a brown solid. The solid material was applied to silica gel and passed through a pad a silica gel along with ethyl acetate (3×50 mL). The filtrate was concentrated to afford N2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amine (0.702 g, 91%). RP-HPLC Rt 18.066 min, 86% purity (5% to 85% acetonitrile/0.1M aqueous ammonium acetate, buffered to pH 4.5, over 20 min at 1 mL/min; λ=254 nm; Deltapak C18, 300 Å, 5 μm, 150×3.9 mm column); m/z 333 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-31a65eb9c2184af09e1d502cb1c8c288 |
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| Source note | uspto-grants-2005_07 |
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