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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075753Generated: November 2, 2026

Dichloromethane → HCID 178523562, compound

https://huagongshe.com/reaction/1075753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-HydroxyphenylglycineHCID 92143—
ReactantHCID 178479697HCID 178479697—
SolventTriethylamineHCID 8471—
ProductHCID 178523562HCID 178523562—

Reaction Steps

To a mixture of 1.35 g of DL- 2-p-hydroxyphenylglycine, 50 ml of anhydrous dichloromethane and 4.05 of triethylamine, 2.62 g of trimethylchlorosilane were added, and the resulting mixture was refluxed for 20 minutes. After the addition of 2.1 g of 4-hydroxy-1,5-naphthyridine-3-carbonyl chloride hydrochloride, the reaction was effected while cooling with ice for 4 hours. The reaction mixture was concentrated under reduced pressure, 50 ml of water were added to the residue, and the resulting mixture was adjusted to pH 1 with 4N hydrochloric acid. The precipitated crystals were collected by filtration, suspended in 50 ml of water and potassium carbonate was added thereto. After removal of insoluble materials by filtration, the filtrate was adjusted to pH 1. The precipitated crystals were collected by filtration, washed with water and dried to give 2.1 g of DL-α-(4-hydroxy-1,5-napthyridine-3-carboxamido)-p-hydroxyphenylacetic acid. M.P. 310° to 320°C (decomp.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954733
Source datasetuspto-grants-1976_05
ORD IDord-59d62368a0d643f7a48eed93af6b418d
Source noteuspto-grants-1976_05