HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514866Generated: October 26, 2026
3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole → HCID 90447582, compound
https://huagongshe.com/reaction/514866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole | HCID 16043572 | — |
| Reactant | HCID 90419021 | HCID 90419021 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 90447582 | HCID 90447582 | 85.4% |
Reaction Steps
A flame-dried vial equipped with a magnetic stir bar was charged with Togni reagent (2.0 g, 7.0 mmol) and CuI (34 mg, 0.35 mmol), and was sealed with a septum. The vial was evacuated and backfilled with N2 for three times. MeOH (8 mL) and tert-butyl 4-acetoxy-4-allylpiperidine-1-carboxylate (4.5 g, 14 mmol) were then added via syringe. The vial was kept at 80° C. for 2 h. The reaction mixture was concentrated in vacuo and the crude residue was purified by a standard method to afford the product (2.1 g). 1H NMR (400 MHz, CHLOROFORM-d) δ: 1.47 (s, 9 H), 1.66-1.77 (m, 2H), 2.00-2.07 (m, 3 H), 2.22 (d, J=13.43 Hz, 2 H), 2.85 (qdd, J=10.61, 10.61, 10.61, 7.25, 1.21 Hz, 2 H), 3.11 (t, J=11.82 Hz, 2 H), 3.81 (br. s., 2 H), 5.58 (dt, J=15.98, 7.19 Hz, 1 H), 6.05 (d, J=16.12 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09108921B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-fd857b52573f4aac9bc718fa6f202713 |
|---|
| Source note | uspto-grants-2015_08 |
|---|