HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129582Generated: October 30, 2026
Triethylamine → N-(8-Methoxychroman-2-yl-methyl)-cyclohexanecarboxamide
https://huagongshe.com/reaction/129582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | HCID 15057554 | HCID 15057554 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(8-Methoxychroman-2-yl-methyl)-cyclohexanecarboxamide | HCID 21843755 | — |
Reaction Steps
A mixture of 9.5 g (49 mmol) of 2-aminomethyl-8-methoxychroman and 4.9 ml (49 mmol) of triethylamine in 50 ml of anhydrous methylene chloride is added dropwise to a solution of 7.2 g (49 mmol) of cyclohexanecarbonyl chloride in 75 ml of anhydrous methylene chloride, while stirring and cooling with ice. After the mixture has been left to stand overnight, it is poured onto ice. Separation of the phases, extraction of the aqueous phase with methylene chloride, washing with saturated sodium chloride solution and drying of the combined organic phases over anhydrous sodium sulphate gives, after evaporation under a water pump vacuum, 14.5 g of crude amide, which is recrystallised from 160 ml of ethyl acetate. IR (KBr): 3307, 2931, 1642, 1485 and 1256 cm
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468882 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-01eba354b94c477a9ed0d9fd67c46f0e |
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| Source note | uspto-grants-1995_11 |
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