HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 6-Chloro-5-methyl-2-pyridinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 6-chloro-5-methylpicolinate | HCID 9837074 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Chloro-5-methyl-2-pyridinemethanol | HCID 10487138 | 73% |
Reaction Steps
0.40 g of sodium borohydride (10.5 mmol) is added in portions to a solution of 1.20 g of 6-chloro-5-methylpyridine-2-carboxylic acid ethyl ester (6.00 mmol) and 10 ml of ethanol maintained at room temperature. The mixture is stirred for 4 hours and then the mixture is poured into an aqueous solution of sodium chloride and the mixture is extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The title product is isolated by chromatography on a silica column (eluent: chloroform). 0.69 g of a colorless oil is recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020345 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-985e6d9e57ba4ff29986cc6b195b8960 |
| Source note | uspto-grants-2000_02 |