HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 58951898, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 58951851 | HCID 58951851 | — |
| Product | HCID 58951898 | HCID 58951898 | — |
Reaction Steps
2,6-Diethyl-3-phenoxy-benzaldehyde was prepared from 2,6-diethyl-3-hydroxy-benzaldehyde and phenylboronic acid in analogy to Example 219a): yellow oil; 1H-NMR (CDCl3): 1.20 (3H, t, CH3), 1.25 (3H, t, CH3), 2.93 (2H, q, CH2), 2.98 (2H, q, CH2), 6.91 (2H, d, 2×ArH), 7.00-7.10 (3H, m, 3×ArH), 7.28-7.38 (2H, m, 2×ArH), 10.6 (1H, s, CHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875645B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-9b5607c5ddf544aba0ebb3cc63a6a2a7 |
| Source note | uspto-grants-2011_01 |