HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-cyclopropyl-6-[(1E)-3-methoxyprop-1-en-1-yl]indan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-[(1E)-3-Methoxyprop-1-en-1-yl]indan-1-one | HCID 67062121 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-cyclopropyl-6-[(1E)-3-methoxyprop-1-en-1-yl]indan-1-amine | HCID 67062179 | — |
Reaction Steps
To a solution of 6-[(1E)-3-methoxyprop-1-en-1-yl]indan-1-one (1 eq.) from the previous step in MeOH (2 M) was added cyclopropylamine (2 eq.) and titanium(IV) isopropoxide (1.3 eq.). The solution was stirred at RT for 1 h before sodium borohydride (1 eq.) was added at 0° C. After 30 min, water was added and the mixture was extracted with ethyl acetate. The combined organic extracts were then washed with water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product by way of flash chromatography (SiO2, Hex→1:9 (v/v) Hex:EtOAc) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889714B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-235e4f76f48d45bbaa5b34e0e1afff49 |
| Source note | uspto-grants-2014_11 |