HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66326Generated: October 30, 2026
Selenium Dioxide → HCID 20434120, compound
https://huagongshe.com/reaction/66326
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 11159836 | HCID 11159836 | — |
| Product | HCID 20434120 | HCID 20434120 | 186.4% |
Reaction Steps
2 g of 2-n-butoxyacetophenone and 1.7 g of selenium dioxide are treated in the same manner as described in Example 6-(1). 2 g of 2-n-butoxyphenylglyoxal thus obtained are dissolved in 6 ml of dimethylsulfoxide, and 1.8 g of 3,4-dimethoxyphenethylamine are added thereto. The solution is stirred at room temperature for 30 minutes. Then, 12 ml of ethanol are added to the solution. After ice-cooling, 0.55 g of sodium borohydride is added gradually to the solution, and the mixture is stirred at room temperature for 1 hour. The reaction mixture is evaporated to remove solvent. Water is added to the thus obtained residue, and the aqueous mixture is extracted with ethyl acetate. The extract is washed with water, dried and then evaporated to remove solvent. The oily residue thus obtained is treated with hydrochloric acid and recrystallized from a mixture of ethanol and ether. 2.6 g of α-(3,4-dimethoxyphenethylaminomethyl)-2-n-butoxybenzylalcohol hydrochloride are obtained. M.p. 128°-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04131686 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-ee1b9928bb5e4b2e992e1a87d80f42cf |
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| Source note | uspto-grants-1978_12 |
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