HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199707Generated: November 2, 2026
Gamma-Butyrolactone → HCID 14051180, compound
https://huagongshe.com/reaction/1199707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Butyrolactone | HCID 7302 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 14051212 | HCID 14051212 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14051180 | HCID 14051180 | 12% |
Reaction Steps
A solution of 1.0 g of 2-(trans-3-aminostyryl)benzothiazole dissolved in 15 ml of anhydrous tetrahydrofuran was cooled to -78° C. and 2.8 ml of a n-hexane solution (1.55M) of n-butyl lithium was added dropwise in a nitrogen gas atmosphere. After a mixture was stirred at the same temperature for 25 minutes, 375 mg of γ-butyrolactone was injected, followed by stirring for 1 hour. After completion of the reaction, the mixture was extracted with ethyl acetate, dried over magnesium sulfate and the solvent was evaporated under reduced pressure. The crude crystals obtained were washed with ethyl ether and dried to obtain 160 mg (yield 12%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04902700 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-5403b0668e1340f8835dfdfb833b381e |
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| Source note | uspto-grants-1990_02 |
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