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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616623Generated: October 29, 2026

Tetrahydrofuran → 61073-23-2

https://huagongshe.com/reaction/616623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantPropionyl chlorideHCID 62324—
Reactant2-Imino-4-methyl-1,3-benzothiazol-3(2H)-amineHCID 20368133—
SolventWaterHCID 962—
Product61073-23-2HCID 20368112—

Reaction Steps

A 3.6 g. portion of 3-amino-2-imino-4-methylbenzothiazoline was dissolved in about 100 ml. of tetrahydrofuran, and 2.2 g. of triethylamine was added. The reaction mixture was cooled in an ice bath, and 2 g. of propionyl chloride, dissolved in 2 ml. of tetrahydrofuran, was added dropwise while the mixture was stirred. After the addition was complete, the reaction mixture was stirred at ice bath temperature for about 3 hours, and was then diluted with an equal volume of water. The tetrahydrofuran was removed under vacuum, and the remaining aqueous mixture was filtered to recover the product. After recrystallization from ethanol, the yield of purified product was 3.2 g. of 3-amino-4-methyl-2-propionyliminobenzothiazoline, m.p. 175°-76° C. The product was identified by nuclear magnetic resonance and ultraviolet analysis and by elemental microanalysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075218
Source datasetuspto-grants-1978_02
ORD IDord-0763091b74c4450393c22745fda122a6
Source noteuspto-grants-1978_02