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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597572Generated: October 30, 2026

Sulfuric Acid → 3'-(2,3,5,6-Tetrahydroimidazo[2,1-b]thiazol-6-yl)acetanilide

https://huagongshe.com/reaction/597572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant3'-[1-Hydroxy-2-(2-imino-3-thiazolidinyl)ethyl]acetanilide hydrochlorideHCID 21445639—
Product3'-(2,3,5,6-Tetrahydroimidazo[2,1-b]thiazol-6-yl)acetanilideHCID 12850512—

Reaction Steps

Addition of 5.00 g. (0.0158 mole) of 3'-[1-hydroxy-2-(2-imino-3-thiazolidinyl)ethyl]acetanilide hydrochloride (Example 6) to 15 ml. of concentrated sulfuric acid is carried out in small increments over 0.5 hour. The orange solution is stirred an additional 1 hour, poured onto ice and made basic with concentrated ammonium hydroxide. The aqueous base is extracted twice with chloroform and the combined organic layers washed with water, brine, dried (sodium sulfate) and evaporated at reduced pressure to give 3.76 g. of an oil. Crystallization from ether gives 3.32 g. (80% crude yield) of fine white crystals, which on recrystallization from 2-propanol gives the product melting point 164°-166° C. Analysis: Calcd. for C13H15N3OS: Calcd: C, 59.74; H, 5.79; N, 16.08; S, 12.27. Found: C, 59.93; H, 5.85; N, 15.96; S, 12.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014892
Source datasetuspto-grants-1977_03
ORD IDord-2584fe792e374fd6b261babaa609145e
Source noteuspto-grants-1977_03