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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378658Generated: November 1, 2026

Pivaloyl chloride → HCID 13154251, compound

https://huagongshe.com/reaction/2378658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant6-Fluoropyridin-2-amineHCID 2761399—
SolventPyridineHCID 1049—
ProductHCID 13154251HCID 1315425193.2%

Reaction Conditions

Temperature0 °C

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) δppm 1.29 (s, 9H), 6.63 (dd, J=8.06, 2.01 Hz, 1H), 7.76 (q, J=8.14 Hz, 1H) ,7.85 (s, 1H), 8.09 (dd, J=8.06, 1.76 Hz, 1H); Mass spec. 197.15 (MH+), Calc. for C10H13FN2O196.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470679B2
Source datasetuspto-grants-2008_12
ORD IDord-d5da50fdd4dc4bbd8a8889b9fd09c2e1
Source noteuspto-grants-2008_12