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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118551Generated: November 2, 2026

Pyridine → HCID 20162855, compound

https://huagongshe.com/reaction/2118551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantPhenoxyacetyl chlorideHCID 69703—
ReactantHCID 14356378HCID 14356378—
SolventDichloromethaneHCID 6344—
ProductHCID 20162855HCID 20162855—

Reaction Steps

A suspension of (23) (830)mg) in dry dichloromethane (20 ml) at -10° C. was treated with triethylamine (220 mg) and pyridine (172 mg), followed by a solution of phenoxyacetyl chloride (372 mg) in dry dichloromethane (~4 ml). The mixture was washed with very dilute HCl, followed by brine. The organic phase was dried and the solvent evaporated. Chromatography on silica yet gave the product (24) (730 mg). νmax (CHCL3) 3400, 1745, and 1690 cm-1 ; δppm (CDCl3) (90 MHz) 0.25 and 0.27 (both s, together 6H), 0.98(S, 9H), 2.22(S, 3H), 3.36 and 3.81 (ABq, 2H, J 7.0 Hz), 4.50(S, 2H), 6.80 to 7.50 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678782
Source datasetuspto-grants-1987_07
ORD IDord-531aff1088c7425cbb5c00f57ec5ed78
Source noteuspto-grants-1987_07