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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231903Generated: October 31, 2026

Ammonium thiocyanate → Ethyl 2-amino-4-bromo-5-thiocyanatobenzoate

https://huagongshe.com/reaction/231903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium thiocyanateHCID 15666—
ReactantBromineHCID 24408—
ReactantHCID 14233599HCID 14233599—
SolventAcetic AcidHCID 176—
ProductEthyl 2-amino-4-bromo-5-thiocyanatobenzoateHCID 14233604—

Reaction Steps

In a 100 ml three-neck round bottom flask equipped with an internal thermometer and magnetic stirrer, a solution of 3.26 g (0.0116 mol) of ethyl 2-amino-4-bromobenzoate hydrochloride, 2.12 g (0.0279 mol) of ammonium thiocyanate and 30 ml of acetic acid was cooled to 15° C. Bromine (1.86 g, 0.0116 mol) was then added dropwise with stirring. A precipitate formed. When the addition was complete, the solution was allowed to warm to room temperature, and to stir for an hour. The product was filtered, dried under nitrogen, and recrystallized from hexane and ethyl acetate to furnish crystalline ethyl 2-amino-4-bromo-5-thiocyanatobenzoate: yield 2.05 g (59%); m.p. 149°-150° C.; ir(KBr) 3487 cm, 3453, 3375, 3346, 2980, 2146, 1697, 1614 among others; 1H-NMR(CDCl3) 1.4 ppm (triplet, 3H, CH2CH3) , 4.3 (quartet, 2H, CH2CH3), 6.0 (broad singlet), 6.9 1H , aromatic H), 8.1 (singlet, 1H aromatic H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849518
Source datasetuspto-grants-1989_07
ORD IDord-e1371c264167419d9a528ec349267675
Source noteuspto-grants-1989_07