HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462097Generated: October 29, 2026
1,2-Dichloroethane → N-(6-Chloromethyl-3,4-methylenedioxyphenethyl) acetamide
https://huagongshe.com/reaction/462097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide | HCID 322384 | — |
| Product | N-(6-Chloromethyl-3,4-methylenedioxyphenethyl) acetamide | HCID 21824570 | — |
Reaction Steps
In a 100 ml round-bottom flask provided with a stirrer, thermometer, gas inlet tube, and a condenser were placed 4.12 g of N-acetyl-homopiperonylamine (0.02 mole), 2.1 g of 37% formaldehyde solution, and 50 ml of ethylene chloride. The mixture was cooled to 3° and hydrogen chloride passed into the stirred mixture. After about 15 minutes a thick paste of crystals had formed. At this point, another 2.1 g of 37% formaldehyde was added and the mixture allowed to stir until all the solid had dissolved. The solution was then poured into ice water and the lower ethylene chloride layer separated, washed three times with water, then dried. The clear ethylene chloride solution was freed of solvent in the rotary evaporator, leaving the above-named product as a crystalline solid. After recrystallization from acetone, the solid melted at 116.5°-122°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04065473 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-ed955b24c7b0443d9df929f54d15de08 |
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| Source note | uspto-grants-1977_12 |
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