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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826682Generated: October 31, 2026

Pyridine → HCID 58635315, compound

https://huagongshe.com/reaction/1826682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosgeneHCID 6371—
ReactantHCID 58635311HCID 58635311—
SolventDichloromethaneHCID 6344—
ProductHCID 58635315HCID 58635315—

Reaction Steps

To a solution of (3R)-3-amino-4-{[tert-butyl(dimethyl)silyl]oxy}butan-1-ol (2.63 g, 12 mmol) in DCM (100 mL) at 0° C. was added pyridine (3 mL) followed by phosgene (20% solution in toluene, 1.9 M, 8.5 mL) dropwise and the mixture was stirred for 30 min and allowed to warm to rt, and quenched with water. The layers were separated and the water layer extracted with DCM once. The organic layers were dried over MgSO4, filtered and concentrated. The desired product (4R)-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1,3-oxazinan-2-one was obtained from crystallization from ether/hexanes at −20° C. as a light yellow solid. 1H NMR (400 MHz, CDCl3) 5.52 (br s, 1H), 4.38–4.33 (m, 1H), 4.28–4.22 (m, 1H), 3.70–3.59 (m, 2H), 3.46 (t, 1H), 1.97–1.93 (m, 1H), 1.72–1.67 (m, 1H), 0.91 (s, 9H), 0.90 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053085B2
Source datasetuspto-grants-2006_05
ORD IDord-f185a6eee13c4e65b6f8b8f032c3af14
Source noteuspto-grants-2006_05