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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448076Generated: October 29, 2026

1-Naphthalenecarbonyl chloride → HCID 69166841, compound

https://huagongshe.com/reaction/448076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenecarbonyl chlorideHCID 70146—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69166841HCID 69166841—

Reaction Steps

In a 20 mL vial 3-butyl-2,4,5-trimethylthiazol-3-ium iodide (48 mg in 0.5 mL DMA, 0.16 mmol, 1 equiv.) was added, followed by TEA (38 mg in 0.5 mL DMA, 0.37 mmol, 2.4 equiv.) and the solution went black. DMAP (2 mg in 0.5 mL DMA, 0.016 mmol, 0.1 equiv) was added next, followed by 1-naphthoyl chloride (0.9 mL of 0.2M in DMA, 1.2 equiv). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.89 (t, 3 H) 1.29-1.39 (m, 2 H) 1.59-1.69 (m, 2 H) 2.26 (s, 6H) 4.02-4.07 (m, 2 H) 6.30 (s, 1 H) 7.50-7.59 (m, 3 H) 7.68-7.71 (m, 1 H) 7.94-8.01 (m, 2 H) 8.30-8.34 (m, 1 H); MS (ESI) m/z 338 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-1c66da8c9fe244bc95d4e95daaeca74c
Source noteuspto-grants-2013_07