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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium ChlorideHCID 433294—
Reactanttert-butyl N-(5-bromo-1,3-thiazol-2-yl)carbamateHCID 21300388—
Producttert-Butyl (5-vinylthiazol-2-yl)carbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-23a0bd2e14de4a5c9b7f308354152055
Source noteuspto-grants-2016_05