HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium thiocyanate → (-)-alpha-Amino-3-(thiocyanatomethyl)-4-hydroxybenzeneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | (-)-alpha-Amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid | HCID 20296136 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (-)-alpha-Amino-3-(thiocyanatomethyl)-4-hydroxybenzeneacetic acid | HCID 23329809 | 78% |
Reaction Steps
A solution of (-)-α-amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid (0.5 g, 1.98 mmole) and potassium thiocyanate (0.4 g, 4.12 mmole) in 10 ml of methanol is stirred at room temperature for 16 hours. The reaction mixture is filtered to remove the potassium chloride, the filtrate is evaporated and to the residue is added saturated aqueous sodium bicarbonate until the pH is 7. The title compound precipitates as a white powder which is filtered and dried. (1.83 g, 78% yield), NMR (TFA-D+D2O) ppm (δ) 4.1 (s,2), 5.08 (s,1), 6.9-7.3 (m,3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229363 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-95b6e6a13b034569841168dbca03942c |
| Source note | uspto-grants-1980_10 |