HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34625Generated: October 29, 2026
Ammonium thiocyanate → Ethyl 2-amino-4-bromo-5-thiocyanatobenzoate
https://huagongshe.com/reaction/34625
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 14233599 | HCID 14233599 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 2-amino-4-bromo-5-thiocyanatobenzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762838 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-daccd96df10842f4b2e90f78e1500398 |
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| Source note | uspto-grants-1988_08 |
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