HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-n-Pentyl-3-(2,4-dichlorophenyl)-allyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-n-Pentyl-3-(2,4-dichlorophenyl)-acrolein | HCID 53822311 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-n-Pentyl-3-(2,4-dichlorophenyl)-allyl alcohol | HCID 54060287 | 61.5% |
Reaction Steps
54.5 g of NaBH4 were added, in portions, to a solution of 150 g of (I) in 1.5 l of methanol. The mixture was refluxed for 1 hour and then concentrated, 1 l of 2N HCl was added, and the mixture was refluxed for a further hour and then extracted with CH2Cl2. The organic phase was washed with water, dried over Na2SO4 and concentrated. Distillation of the residue gave 93 g of (II) of boiling point 156°-160° C./0.2 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472412 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-f00997a6b580433c94373ce5b12f620f |
| Source note | uspto-grants-1984_09 |