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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883942Generated: November 3, 2026

Pyridine → HCID 23508700, compound

https://huagongshe.com/reaction/1883942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(Hydroxymethyl)benzoic acidHCID 76360—
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ProductHCID 23508700HCID 23508700—

Reaction Steps

A solution of commercial 4-(hydroxymethyl)benzoic acid (1.52 g, 10.0 mmol) in pyridine (50 mL) is treated with 4,4′-dimethoxytrityl chloride (3.73 g, 11.0 mmol) overnight at room temperature and concentrated to an oil in vacuo. The residue is dissolved in a mixture of MeOH and CH2Cl2 (95:5, v/v; 200 mL) and washed with 2 M aqueous triethylammonium acetate (5×20 mL). The organic solution is evaporated, re-dissolved in CH2Cl2, dried over Na2SO4, and evaporated to give crude triethylammonium 4-[[(4,4′-dimethoxytrityl)oxy]methyl]-benzoate in quantitative yield (1016 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762281B2
Source datasetuspto-grants-2004_07
ORD IDord-7e794dbb1b204d3f85f63cefe75aa15d
Source noteuspto-grants-2004_07