HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265071Generated: October 28, 2026
1-Bromo-3-chloropropane → 3-[(3-Chloropropyl)thio]-4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-4H-1,2,4-triazole
https://huagongshe.com/reaction/2265071
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-Methyl-3-(4-methyloxazol-5-yl)-1H-1,2,4-triazole-5(4H)-thione | HCID 10420204 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[(3-Chloropropyl)thio]-4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-4H-1,2,4-triazole | HCID 44627994 | — |
Reaction Steps
NaOEt (21% solution in EtOH, 2.08 vol, 1.1 eq) was added to EtOH (20 vol) under nitrogen atmosphere. 4-Methyl-5-(4-methyl-1,3-oxazol-5-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (respectively a tautomeric form thereof; 290 g, 1 wt) was added in one portion and the resulting mixture stirred at 25±2° C. until a clear solution was obtained. Then 1-bromo-3-chloropropane (0.54 vol, 1.1 eq) was added and the solution stirred at 40° C. for 24 h then cooled to 25° C. After filtration water (20 vol) was added and the ethanolic phase was removed by vacuum distillation (internal temperature ˜40° C.). The mixture was extracted with EtOAc (41 vol). The aqueous layer was removed and the organic phase was evaporated to dryness. Dichloromethane (4 vol) was added. The organic solution is purified through a short silica gel column (18 wt of silica), eluting with EtOAc (200 vol) to give the title compound as a solid foam (267.64 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855298B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-59d7ac029101446797429c7df127a2cf |
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| Source note | uspto-grants-2010_12 |
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