HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 21479357, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 21479360 | HCID 21479360 | — |
| Product | HCID 21479357 | HCID 21479357 | — |
Reaction Steps
Following the procedure of Example 1(a)-1(c) except substituting 4-methylphenylboronic acid for phenylboronic acid in step (b), and the procedure of Example 9(a), except substituting ethyl 5-benzyloxy-1-(2-chloro-4,5-methylenedioxybenzyl)-3-(4-methylphenyl)indole-2-carboxylate for ethyl 5-benzyloxy-1-(2-chloro-4,5-methylenedioxybenzyl)-3-phenylindole-2-carboxylate, the title compound was prepared as a white solid (0.304 g, 81%). 1HNMR (400 MHz, CDCl3) δ 7.37 (m, 2H), 7.24 (s, 1H), 7.15 (d, 1H), 6.97 (m, 3H), 6.00 (s, 1H), 5.89 (s, 2H), 5.71 (s, 2H), 4.56 (s, 1H), 4.13 (q, 2H), 2.43 (s, 3H), 1.03 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05684032 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-3911ab82eac4462e99f546bfc10a94a8 |
| Source note | uspto-grants-1997_11 |