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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905651Generated: November 3, 2026

Pyridine → HCID 20162855, compound

https://huagongshe.com/reaction/1905651

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 (boths, 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 numberUS04647558
Source datasetuspto-grants-1987_03
ORD IDord-c343dd2632774a4b8eb326113f810fb6
Source noteuspto-grants-1987_03