Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | HCID 14371620 | HCID 14371620 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14371619 | HCID 14371619 | — |
Reaction Steps
A mixture of 1.0 grams(3.65 mmol) of Compound L from step B, 0.55 mL (3.65 mmol) 2-bromoacetaldehyde diethyl acetal, and 1.0 grams (7.3 mmol) anhydrous potassium carbonate in 35 mL dry DMF was stirred at 150° C. for 4 hours. After cooling to room temperature, the mixture was poured into 300 mL ether, washed with three 50 mL portions of water, dried (MgSO4) and evaporated. The residue was purified by flash chromatography, eluting with 1:1 hexane-ethyl acetate to give 1.1 grams (77%) of N-(2,2-diethoxyethyl)-trans-1-(3-methoxy-4-chlorophenyl-2-indanamine (Compound M) as an oil, 200 MHz NMR(CDCl3) d 1.15(tr,6H,J=7 Hz), 2.70-290(m,3H), 3.20-3.70(m,6H), 4.09(d,1H,J=8 Hz), 4.55(tr,1H,J=5 Hz), 6.70-6.90(m,3H), 7.10-7.30(m,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302716 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-1408ff0ff5024cd08ae3e001e631f764 |
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| Source note | uspto-grants-1994_04 |
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