HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 15431542, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15166220 | HCID 15166220 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15431542 | HCID 15431542 | 95.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
0.71 g (6 mmol) of thionyl chloride was added to a solution of 0.40 g (1.5 mmol) of 2-hydroxymethyl-3-methyl-4-(2-pyridylmethoxyethoxy)pyridine in 10 ml of chloroform under cooling with ice to obtain a mixture. This mixture was stirred at 0° C. for 2 hours. After the completion of the reaction, the mixture was neutralized with a saturated aqueous solution of sodium hydrogencarbonate and extracted with 50 ml of chloroform four times. The extract was dried over magnesium sulfate and filtered. The obtained filtrate was concentrated and dried in a vacuum to obtain 0.42 g of crude 2-chloromethyl-3-methyl-4-(2-pyridylmethoxyethoxy)pyridine as a semicrystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840910 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-556251424eab45c5ad07e8e587220241 |
| Source note | uspto-grants-1998_11 |