HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2H-1,3-benzodioxol-5-yl)boronic acid → HCID 13354023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2H-1,3-benzodioxol-5-yl)boronic acid | HCID 2734371 | — |
| Reactant | 3-Bromocyclohex-2-enone | HCID 10965038 | — |
| Product | HCID 13354023 | HCID 13354023 | 85% |
Reaction Steps
Synthesized from 3-bromocyclohex-2-enone and 3,4-methylenedioxyphenylboronic acid according to the general procedure described for the Suzuki coupling. Purification by automated flash chromatography using gradient elution (0 to 80% ethyl acetate/hexanes) yielded the product (164 mg, 85%) as a white solid. 1H NMR (300 MHz, CDCl3): δ 7.07-7.00 (m, 2H), 6.81 (d, J=8.0 Hz, 2H), 6.31 (s, 1H), 5.99 (s, 2H), 2.70 (t, J=5.5 Hz, 2H), 2.45 (t, J=6.3 Hz, 2H), 2.12 (quintet, J=6.3 Hz, 2H). 13C (75 MHz, CDCl3): 199.7, 159.0, 149.2, 148.2, 132.8, 124.2, 120.7, 108.4, 106.3, 101.6, 37.4, 28.3, 23.0. LCMS (ESI): mass calcd for (C13H12O3) m/z 216.08; measured [M+H]+: m/z 216.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003692B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-8067ae5d589c451e860986313d16f720 |
| Source note | uspto-grants-2011_08 |