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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356503Generated: October 31, 2026

Pyridine → HCID 20586035, compound

https://huagongshe.com/reaction/1356503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantLeucine methyl ester hydrochlorideHCID 2723695—
SolventDichloromethaneHCID 6344—
ProductHCID 20586035HCID 2058603586%

Reaction Conditions

Temperature0 °C

Reaction Steps

L-leucine methyl ester hydrochloride (25 g, 0.14 mol) was dissolved in methylene chloride (450 mL), cooled to 0° C., and pyridine (43.5 g, 0.55 mol, 44.5 mL) was added, then a 1.93 M solution of phosgene in toluene (0.18 mol, 92.7 mL) was added slowly. After stirring at 0° C. for 2 h, the mixture was poured into 1400 mL of 0.5 N Hcl and 900 mL of ice. The organic layer was washed with 1400 mL of 0.5 N Hcl and 900 mL of ice. The aqueous layers were extracted with methylene chloride (450 mL) and the combined organic layers were washed with 1400 mL of saturated brine and 900 mL of ice, then dried (MgSO4), filtered and concentrated. The residue was distilled (56-58° C.; 0.78 mmHg) to provide the title compound as a colorless liquid (20.4 g, 86%). 1H NMR (250 MHz, CDCl3) δ4.04 (dd, 1H), 3.82 (s, 3H), 1.92-1.72 (m, 1H), 1.69-1.62 (m, 2H), 0.96 (d, 3H), 0.94 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586466B2
Source datasetuspto-grants-2003_07
ORD IDord-6906c37b808645edb38fa6878df83165
Source noteuspto-grants-2003_07