HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexamethylenetetramine → 3-(4-Formyl-benzooxazol-2-yl)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Acetic acid--water (1/1) | HCID 21899381 | — |
| Reactant | 3-(4-Bromomethyl-benzooxazol-2-yl)-benzoic acid methyl ester | HCID 67279350 | — |
| Product | 3-(4-Formyl-benzooxazol-2-yl)-benzoic acid methyl ester | HCID 86066106 | 32% |
Reaction Steps
The crude 3-(4-bromomethyl-benzooxazol-2-yl)-benzoic acid methyl ester is treated with HMTA (1.8 mmol) in acetic acid/H2O (3 mL/1.5 mL) in a microwave oven at 130° C. for 20 minutes. The solvent is removed and the mixture is purified by silica gel chromatography (10-20% EtOAc/hexane) to yield 3-(4-formyl-benzooxazol-2-yl)-benzoic acid methyl ester as a white solid. Yield: 32%. 1H NMR (400 MHz, CDCl3) 10.8 (s, 1H), 8.97 (s, 1H), 8.53 (d, J=7.8 Hz, 1H), 8.26 (d, J=7.8 Hz, 1H), 7.94 (dd, J1=7.7 Hz, J2=1 Hz, 1H), 7.86 (d, J=8.1 Hz, 1H), 7.66 (t, J=7.8 Hz, 1H), 7.51 (t, J=7.9 Hz, 1H), 4.0 (s, 3H). LC/MS (ES+): (M+1) 282.1, (M+Na) 304.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158662B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-dc455e9d46a74a8e9c2de4ef374c99ac |
| Source note | uspto-grants-2012_04 |