HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-Chloro-1-(2-thienyl)-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Chloro-1-(2-thienyl)-1-propanone | HCID 7567855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Chloro-1-(2-thienyl)-1-propanol | HCID 11658374 | — |
Reaction Steps
For example, a method is known wherein 1-(2-thienyl)-3-chloropropan-1-one is reduced using sodium borohydride in ethanol to obtain 3-chloro-1-(2-thienyl)-1-propanol, halogen exchange is subsequently conducted in acetone using sodium iodide to obtain 3-iodo-1-(2-thienyl)-1-propanol, and then this is reacted with a monomethylamine aqueous solution in tetrahydrofuran (CHIRALITY, 12, 26-29 (2000)). However, since the raw material used in this method is 1-(2-thienyl)-3-chloropropan-1-one, which is a very unstable compound, this method is not industrially applicable.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722906B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-4468c15f9511432f9b12f9e957049382 |
| Source note | uspto-grants-2014_05 |