HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22708810 | HCID 22708810 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)methanol | HCID 11264156 | 87.6% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
1-(Phenylmethyl)4-(hydroxymethyl)-pyridinyl chloride(0.87 mol) was dissolved in methanol (2200 ml) and cooled to −20° C. Sodium borohydride (1.75 mol) was added portionwise under a nitrogen atmosphere. The reaction mixture was stirred for 30 minutes and water (200 ml) was added dropwise. The reaction mixture was partially evaporated, water was added and the reaction mixture was extracted with DCM. The organic layer was separated, dried, filtered and evaporated. The residue was purified over silica gel (eluent: DCM), yielding 155 g of 1,2,3,6-tetrahydro-1-(phenylmethyl)4-pyridinemethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06544997B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-73334193d9d84a0d8708a39fcc3cd3ce |
| Source note | uspto-grants-2003_04 |