HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 6-(Chloromethyl)isoquinoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Hydroxymethyl)quinoline | HCID 80479 | — |
| Product | 6-(Chloromethyl)quinoline hydrochloride | HCID 20081969 | — |
| Product | 6-(Chloromethyl)isoquinoline hydrochloride | HCID 68182281 | 93% |
Reaction Steps
To a solution of quinolin-4-ylmethanol MDE 32046 (0.24 g, 1.51 mmol) in dry CH2Cl2 (10 mL) at 0° C. under N2 in a 50 mL round-bottomed flask equipped with a magnetic stirrer was added dropwise SOCl2 (2.3 mL, 31.2 mmol) and the mixture was stirred for 1 h at RT. The volatiles were then removed at 40° C. under vacuum and the residue was taken up in CH2Cl2 (20 mL) before concentration back to dryness at 40° C. under vacuum (done 3 times) to give 6-(chloromethyl)quinoline hydrochloride MDE 32048 as an off-white solid (301 mg, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772316B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-da02cedbe64f49a994cf13afefdb86c5 |
| Source note | uspto-grants-2014_07 |