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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073946Generated: October 31, 2026

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

https://huagongshe.com/reaction/2073946

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 (singlet, 1H, aromatic H), 8.1 (singlet, 1H aromatic H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920224
Source datasetuspto-grants-1990_04
ORD IDord-ca69be11f6d246638f5f51120dcee81a
Source noteuspto-grants-1990_04