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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358780Generated: October 31, 2026

HCID 69632012, compound → HCID 53826150, compound

https://huagongshe.com/reaction/1358780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69632012HCID 69632012—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductHCID 53826150HCID 53826150103.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596772B1
Source datasetuspto-grants-2003_07
ORD IDord-8b797fb3640242009e40c760a234fbb7
Source noteuspto-grants-2003_07