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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3'-[1-Hydroxy-2-(2-imino-3-thiazolidinyl)ethyl]acetanilide hydrochloride | HCID 21445639 | — |
| Product | 3'-(2,3,5,6-Tetrahydroimidazo[2,1-b]thiazol-6-yl)acetanilide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04014892 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-2584fe792e374fd6b261babaa609145e |
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| Source note | uspto-grants-1977_03 |
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