HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358780Generated: October 31, 2026
HCID 69632012, compound → HCID 53826150, compound
https://huagongshe.com/reaction/1358780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69632012 | HCID 69632012 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53826150 | HCID 53826150 | 103.3% |
Reaction Steps
Dissolved 1.2 g (4 mmol) of 6-Hydroxymethyl-2-naphthalenecarboxylic acid benzyl ester in 100 ml of CH2Cl2, slowly added 5.2 g of MnO2 (60 mmol) and stirred at room temperature for 2 hours, then filtered through Ceilite. The Celite was washed with CH2Cl2 and combined organics taken to dryness. The oily residue was solidified with EtOAc/Hexanes (1:1) and collected by vacuum filtration, washed with small amount of methanol, dried to get 1.2 g of 6-Formyl-2-naphthalenecarboxylic acid benzyl ester. 1H NMR (400 MHz, DMSO-d6): δ 10.192 (s, 1H, —CHO), 8.754 (s, 1H, Ar—H), 8.667 (s, 1H, Ar—H), 8.327(t, J=9.4, 2H, Ar—H), 8.142(dd, J=1.6&7.0 Hz, 1H, Ar—H), 7.987-7.962 (dd, J=1.6&7.0 Hz, 1H, Ar—H), 7.544-7.526 (m, 2H, Ar—H), 7454-7.375 (m, 3H, Ar—H), 5.442 (s, 2H, —COOCH2—), MS m/e 289[M+−1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06596772B1 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-8b797fb3640242009e40c760a234fbb7 |
|---|
| Source note | uspto-grants-2003_07 |
|---|