HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421916Generated: October 31, 2026
2-Naphthoic acid → 2-Naphthalenecarbonyl isothiocyanate
https://huagongshe.com/reaction/1421916
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Naphthoic acid | HCID 7123 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Naphthalenecarbonyl isothiocyanate | HCID 2113413 | 84.1% |
Reaction Steps
To a mixture of 2-naphthyl carboxylic acid (5.0 g, 29.0 mmol) and 2 drops of N,N'-dimethylformamide in dry tetrahydrofuran (50 ml) was added dropwise thionyl chloride (6.3 ml, 87 mmol) and the resulting reaction mixture was stirred at reflux temperature for 3 h. The volatiles were evaporated in vacuo and the solid residue was redissolved in dry tetrahydrofuran (30 ml) and added dropwise to a solution of potassium thiocyanate (2.9 g, 30 mmol) in acetone (40 ml). The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was quenched with water (250 ml) and extracted- with diethyl ether (2×100 ml). The combined organic extracts were washed with saturated aqueous sodium chloride (2×80 ml), dried (MgSO4), filtered and evaporated in vacuo affording 5.2 g (84%) of naphthalene-2-carbonyl isothiocyanate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080770 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-f5abd7c6d20740f6bc7257378cbf6b73 |
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| Source note | uspto-grants-2000_06 |
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