HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741653Generated: October 30, 2026
Hexamethylphosphoramide → 3-Methyl-5-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]thiazole
https://huagongshe.com/reaction/741653
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-[4-(2-Methyltetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide | HCID 15391523 | — |
| Reactant | 3-Methyl-thiazole | HCID 15407522 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-5-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]thiazole | HCID 22103454 | 28% |
Reaction Steps
n-BuLi (2.5M, 1.33 ml, 3.33 mmol) was added slowly at -78° C. to a solution of 3-methyl-thiazole (300 mg, 3.03 mmol) in 8 ml of THF under nitrogen. After stirring at -78° C. for 15 min, HMPA (1.08 g, 6.06 mmol) was added and the resulting mixture was stirred for 10 min. To the above mixture was added at -78° C. 3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide (985 mg, 3.03 mmol) in 5 ml of THF. The mixture was allowed to warm to 20° C. and stirred for 3 h. Saturated ammonium chloride solution was added and the aqueous layer was extracted with ether (3×), and the organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica column chromatography (15 cm column, ethyl acetate/hexane, 1/8-3/1) to afford 290 mg (28%) of 3-methyl-5-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05552420 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-50f5cc3d412e452ca88510e6ad56ad3b |
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| Source note | uspto-grants-1996_09 |
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