HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903184Generated: November 2, 2026
1,2-Dichloroethane → Ethanol, 2-(cyclohexylamino)-
https://huagongshe.com/reaction/1903184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | Ethanol, 2-(cyclohexylamino)- | HCID 17827 | — |
Reaction Steps
Into 100 g of cyclohexylamine was added 41 g of ethylene chloride and the mixture was stirred at about 160° C. for 10 hours. After cooling the reaction mixture to a room temperature, 100 ml of 10 N-NaOH aqueous solution was added to the reaction mixture and the organic layer was obtained by using a separating funnel and thus obtained organic layer was dried with KOH. KOH was removed by filtration and the mother liquor was distilled under a reduced pressure. 48 Grams of N-(2-hydroxyethyl)cyclohexylamine was obtained as an oily substance. Boiling point: 132°-135° C. (18 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435404 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-3fe0b6c7f5a14e6ab91937a2840f7b2d |
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| Source note | uspto-grants-1984_03 |
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