HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66461Generated: October 30, 2026
Sodium Sulfate → 2-Amino-1-(3,4-dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)heptane
https://huagongshe.com/reaction/66461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 1-(3,4-Dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)-2-nitroheptane | HCID 13065021 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-1-(3,4-dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)heptane | HCID 13588847 | — |
Reaction Steps
To a suspension of 6.6 g. (0.174 mole) of LiAlH4 in 200 ml. of dry tetrahydrofuran was added dropwise a solution of 25 g. (0.058 mole) of 1-(3,4-dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)-2-nitroheptane in 100 ml. of dry THF at room temperature at such a rate as to control reflux of reaction solution. After addition of substrate was completed, the reaction mixture was refluxed under N2 for 2 hours, and cooled to ice bath temperature. The excess LiAlH4 was decomposed with saturated Na2SO4 solution. The inorganic salt was filtered off and thoroughly washed with ethyl acetate and chloroform. The filtrate was concentrated in vacuo to give 28 g. of brown, oily product. Without further purification, the amino ketal derivative was used for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04342692 |
|---|
| Source dataset | uspto-grants-1982_08 |
|---|
| ORD ID | ord-0bd7cac034574275b3375b8afcda26ac |
|---|
| Source note | uspto-grants-1982_08 |
|---|