HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215711Generated: October 29, 2026
Sodium Hydroxide → ((2,3-Dimethylphenyl)methyl)-1,3-thiazolin-2-ylamine
https://huagongshe.com/reaction/215711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ((2,3-Dimethylphenyl)methyl)-1,3-thiazolin-2-ylamine hydrochloride | HCID 68955163 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | ((2,3-Dimethylphenyl)methyl)-1,3-thiazolin-2-ylamine | HCID 57569039 | 99.6% |
Reaction Steps
A mixture of 1.4 grams (0.034 mole) of sodium hydroxide in 100 mL of water was added to a stirred, cold (ice water bath) mixture of 8.0 grams (0.031 mole) of ((2,3-dimethylphenyl)methyl)-1,3-thiazolin-2-ylamine hydrochloride (Compound C11) in 100 mL of diethyl ether. The reaction mixture was allowed to warm to ambient temperature where it stirred for two hours. The reaction mixture was poured into a separatory funnel and the organic phase was removed and saved. The aqueous phase was extracted with 100 mL of diethyl ether. The organic extract was combined with the saved organic phase, dried with sodium sulfite and filtered. The filtrate was concentrated under reduced pressure to yield 6.8 grams of the title compound as a white solid, melting point 110-114° C. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193118B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-0a74d17aec6e4360a8b38730d97d3d46 |
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| Source note | uspto-grants-2012_06 |
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