HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 23138794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23138831 | HCID 23138831 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23138794 | HCID 23138794 | 37% |
Reaction Steps
(E)-3-({2-[3-(Ethoxycarbonyl)propyl]-2H-tetrazol-5-yl}methylidene)-1-(triphenylmethyl)piperidin-4-one (3.93 g) was reduced with sodium borohydride (281 mg) in a mixed solvent of dichloromethane (30 ml) and ethanol (30 ml) in a similar manner to that mentioned in Example 138 (c), and the crude product obtained by conventional extraction procedures was purified by chromatography on silica gel using a mixture of ethyl acetate and hexane (1:9 to 7:3) as the eluent to afford the title compound as a yellow oil (1.46 g, yield: 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829580B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-5c59255ba917438a828f7e09d6cae192 |
| Source note | uspto-grants-2010_11 |