HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457992Generated: October 29, 2026
Diisopropylethylamine → HCID 18468203, compound
https://huagongshe.com/reaction/457992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Fluoro-2-hydroxybenzoyl chloride | HCID 18468127 | — |
| Reactant | Acetonitrile--hydrogen chloride (1/1) | HCID 22261314 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18468203 | HCID 18468203 | 65% |
Reaction Steps
A solution of 4-fluorosalicylic acid chloride (Example 1, 10 g, 57.3 mmol) in dichloromethane (114 mL) was treated with N,N-diisopropylethyl amine (25 mL, 143 mmol) and acetonitrile hydrochloride (7.95 g, 85.9 mmol). After stirring at 35° C. for 24 h, the solution was concentrated under reduced pressure, diluted with ethyl acetate, and washed successively with 2 N HCl and saturated aq NaCl. The resulting solution was dried over MgSO4, filtered and concentrated. The resulting solid was suspended in dichloromethane, filtered and rinsed with heptane to give N-cyanomethyl-4-fluoro-2-hydroxy-benzamide (7.20 g, 65%): 1H NMR (DMSO-d6 300 MHz) δ 12.16 (br s, 1 H), 9.17 (t, J=5.3 Hz, 1 H), 7.88 (dd, J, =8.7 Hz, J2=6.3 Hz, 1 H), 6.81–6.73 (m, 2 H), 4.32 (d, J=5.7 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189749B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d541495d1e6d498c84c702e372ada1e4 |
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| Source note | uspto-grants-2007_03 |
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