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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942637Generated: November 3, 2026

Bromine → 5-(5-Bromo-thiazol-2-yl)-2-isopropoxybenzonitrile

https://huagongshe.com/reaction/1942637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant2-Isopropoxy-5-thiazol-2-ylbenzonitrileHCID 57506028—
SolventAcetic AcidHCID 176—
Product5-(5-Bromo-thiazol-2-yl)-2-isopropoxybenzonitrileHCID 57506029—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 2-[(1-methylethyl)oxy]-5-(1,3-thiazol-2-yl)benzonitrile (D64) (215 mg) and sodium acetate (144 mg) in acetic acid (8 mL) stirred at room temperature was added a solution of Br2 (0.045 mL) in acetic acid (1 mL) dropwise. The reaction mixture was stirred at 20° C. until start material was consumed completely. The reaction mixture was basified with 2M NaOH, then diluted with ethyl acetate. The mixture was washed with water and brine. The organic phase was dried over anhydrous sodium sulphate. After concentration, the crude product 5-(5-bromo-1,3-thiazol-2-yl)-2-[(1-methylethyl)oxy]benzonitrile (D65) (320 mg) was used for next step without further purification. δH (CDCl3, 600 MHz): 1.36 (6H, d), 4.65 (1H, m), 6.95 (1H, d), 7.64 (1H, s), 7.92 (1H, d), 7.97 (1H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-2cb45aae571f42b9af11281a84663bb9
Source noteuspto-grants-2013_03