HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656357Generated: October 29, 2026
Hydrochloric Acid → HCID 18440313, compound
https://huagongshe.com/reaction/656357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 6-Bromo-2-tetralone | HCID 2733553 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18440313 | HCID 18440313 | 70% |
Reaction Steps
A mixture of 6-bromo-2-tetralone (1.00 g, 4.44 mmol) and methylamine hydrochloride (300 mg, 4.44 mol) in H2O (1 mL) and EtOH (1.5 mL) was stirred at ambient temperature for 20 min. Potassium cyanide (289 mg, 4.44 mmol) was added and stirring was continued for 18 h. The mixture was added dropwise to a stirred solution of 1.0 N aqueous HCl (4.5 mL) at 0° C., then potassium cyanate (360 mg, 4.44 mmol) was added portionwise. The stirred mixture was heated to 95° C. and conc. hydrochloric acid (0.44 mL) was added dropwise. The reaction mixture was heated at this temperature for 1 h, allowed to cool, and extracted with CH2Cl2 (80 mL). The organic extract was dried over Na2SO4, filtered, and concentrated to dryness. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 90:10, to provide a crude sample of the title compound (ca. 70% pure). Trituration with EtOH afforded the title compound. MS: m/z=311 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071770B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-5c6f2e3a81e9409f9807c145ca57cc15 |
|---|
| Source note | uspto-grants-2011_12 |
|---|