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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296684Generated: October 31, 2026

Pyridine → HCID 5327772, compound

https://huagongshe.com/reaction/2296684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 54298240HCID 54298240—
SolventDiethyl EtherHCID 3283—
ProductHCID 5327772HCID 5327772—

Reaction Steps

To a stirred ice-cooled solution of 167 mg of 6-amino-3-chloro-α-(1-butynyl)-α-(trifluoromethyl)benzyl alcohol in 15 mL of dry ether was added 0.100 mL of dry pyridine and 0.066 mL of bromoacetyl bromide. After 30 min, the reaction mixture was diluted with ether, washed with water and aqueous sodium bicarbonate, dried and evaporated. The residue was dissolved in 15 mL of dry DMF and was treated at room temperature with 25 mg of 100% sodium hydride for 1.5 h. The reaction was partitioned between ethyl acetate and water and the ethyl acetate layer was washed with brine, dried and evaporated. The crude product was purified by preparative silica gel TLC (elution with ethyl acetate/hexanes 1:2) affording after crystallization from ethyl acetate/hexanes 106 mg of the title compound as colorless crystals: mp 167-168°; Anal. Calcd. for C14H11NO2ClF3: C, 52.93; H, 3.49; N, 4.42. Found: C, 52.73; H, 3.64; N, 4.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489320B1
Source datasetuspto-grants-2002_12
ORD IDord-bc68a18980654baca175290cf1bc31c3
Source noteuspto-grants-2002_12