HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dichloroethane → HCID 86606925, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Oxa-8-azaspiro(4.5)decane hydrochloride | HCID 21955264 | — |
| Reactant | HCID 86601740 | HCID 86601740 | — |
| Product | HCID 86606925 | HCID 86606925 | — |
Reaction Steps
A mixture of 2-[1-{(2R,3R,4R)-2-[(1R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy]-3-(4-fluorophenyl)-tetrahydropyran-4-carbaldehyde (Description 11; 0.15 g, 0.32 mmol), 2-oxa-8-azaspiro[4.5]decane hydrochloride (0.85 g, 0.48 mmol), triethylamine (50 μL, 0.49 mmol), sodium triacetoxyborohydride (0.136 g, 0.64 mmol) and dichloroethane (3 ml) was stirred at room temperature for 2 hours. The mixture was treated with sodium bicarbonate and extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by chromatography on alumina (grade III) using ethyl acetate in hexane (10-50%) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393858B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-9fc377742abb402c9980a21199564eef |
| Source note | uspto-grants-2008_07 |