HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524401Generated: October 30, 2026
Dimethylformamide → tert-Butyl (5-vinylthiazol-2-yl)carbamate
https://huagongshe.com/reaction/524401
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | tert-butyl N-(5-bromo-1,3-thiazol-2-yl)carbamate | HCID 21300388 | — |
| Product | tert-Butyl (5-vinylthiazol-2-yl)carbamate | HCID 53486835 | — |
Reaction Steps
(5-Bromo-thiazol-2-yl)-carbamic acid tert-butyl ester (0.200 g, 0.71 mmol), tetrakis(triphenylphospine)palladium (0.042 g, 0.036 mmol), lithium chloride (0.91 g, 2.14 mmol), and tributyl (vinyl)stannate (0.68 g, 2.14 mmol) were taken in 8 mL of THF and 8 mL of DMF and reflux for 2 hrs. After completion of reaction THF was removed under reduced pressure on ratavapour and the residue was partioned between ethyl acetate (20 mL) and water (20 mL). The layers were separated. Aq. Layer was extracted with ethyl acetate (2×20 mL). The combined organic layer was washed with brine and dried over anhydrous sodium sulfate filtered and concentrated under reduced pressure to get the crude product which was purified by preparative TLC to get the pure product (5-Vinyl-thiazol-2-yl)-carbamic acid tert-butyl ester (0.137 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340506B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-23a0bd2e14de4a5c9b7f308354152055 |
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| Source note | uspto-grants-2016_05 |
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