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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351854Generated: November 4, 2026

Iodine → HCID 14651914, compound

https://huagongshe.com/reaction/2351854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 72738199HCID 72738199—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 14651914HCID 14651914—

Reaction Steps

In a stream of argon, 182 ml of dry methanol, 191 ml of dry ether and 38.5 g (0.279 mole) of potassium carbonate were added to 31.0 g (0.140 mole) of 3-amino-4-benzyloxy-2-butenethioamide obtained in Referential Example 4, and under heating and reflux, a solution of 26.6 g (0.209 mole) of iodine in dry ether 191 ml was added droopwise to the mixture. Then, the mixture was refluxed for 1.5 hours, and 130 ml of dry ether containing 17.7 g (0.140 mole) of iodine was added dropwise under reflux. After cooling, water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed successively with water, an aqueous solution of sodium thiosulfate and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The resulting 5-amino-3-benzyloxymethyl isothiazole was subjected to silica gel column chromatography, and the column was eluted with chloroform/methanol (500/2) to give 25.5 g (83.0%) of a brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874760
Source datasetuspto-grants-1989_10
ORD IDord-7c7a04c8cfad412699985a65777b9a7d
Source noteuspto-grants-1989_10