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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283317Generated: October 31, 2026

Tetrahydrofuran → 61073-23-2

https://huagongshe.com/reaction/1283317

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 numberUS03974286
Source datasetuspto-grants-1976_08
ORD IDord-ee0622ee021e4c978a80b09ae497d49e
Source noteuspto-grants-1976_08