HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132234Generated: October 31, 2026
Pivaloyl chloride → HCID 13154251, compound
https://huagongshe.com/reaction/132234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 6-Fluoropyridin-2-amine | HCID 2761399 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13154251 | HCID 13154251 | 93.2% |
Reaction Steps
6-fluoropyridin-2-amine (13.1 g, 117 mmol) was dissolved in anhydrous pyridine (100 mL), and cooled to 0° C. followed by fast dropwise addition of trimethylacetyl chloride (15.9 mL, 129 mmol) over 2 min. 5 min later, the resulting slurry was stirred over night at room temperature. Partial of the solvent was removed on rotary vacuum. The residue was partitioned between saturated ammonium chloride (200 mL) and EtOAc (200 mL). After separation, the organic layer was washed with brine (50 mL), dried over MgSO4, concentrated on rotary vacuum, and purified on flash chromatography eluting with 25˜75% EtOAc/Hexanes (1400 mL) to afford the expected product as a white solid(21.4 g, 93% yield); 1H NMR (400 MHz, CDCl3) δ ppm 1.29 (s, 9 H), 6.63 (dd, J=8.06, 2.01 Hz, 1 H), 7.76 (q, J=8.14 Hz, 1 H), 7.85 (s, 1 H), 8.09 (dd, J=8.06, 1.76 Hz, 1 H); Mass spec. 197.15 (MH+), Calc. for C10H13FN2O196.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384930B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-6a40b07d6de843328a0fb3f8f0133177 |
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| Source note | uspto-grants-2008_06 |
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