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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589484Generated: October 31, 2026

Methanol → HCID 13178451, compound

https://huagongshe.com/reaction/1589484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 86740071HCID 86740071—
SolventDiethyl EtherHCID 3283—
ProductHCID 13178451HCID 13178451—

Reaction Steps

To a suspension of 3.0 g of 5-amidinosalicylic acid methanesulfonate in 40 ml of dried pyridine, while being cooled in ice and stirred, was added slowly 1.5 g of benzoyl chloride. The mixture was stirred for 3 hours at room temperature. The crystals gradually dissolved, forming a clear pale yellow solution, and an oily substance separated out. After addition of ethyl ether to the reaction mixture and removal of the supernatant, the oily substance was washed several times with ethyl ether and dissolved in water. Upon addition of a saturated aqueous sodium hydrogencarbonate solution, pale yellow crystals precipitated. After cooling in ice, the crystals were collected by filtration, washed with a small volume of water, and dried to obtain 1.0 g of the crystals. The crystals were suspended in a small volume of methanol and allowed to dissolve by the addition of 0.4 g of methanesulfonic acid. Ethyl ether was added to the solution with stirring to obtain 0.8 g of a colorless powder of 4-amidino-2-carboxyphenyl benzoate methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04570006
Source datasetuspto-grants-1986_02
ORD IDord-d398c81175ce49f280121f7ec13047c2
Source noteuspto-grants-1986_02