HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268516Generated: October 31, 2026
1-Chloro-2-(diethylamine)ethane hydrochloride → 2,7-Bis(2-diethylaminoethoxy)fluorene dihydrochloride
https://huagongshe.com/reaction/268516
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-2-(diethylamine)ethane hydrochloride | HCID 13363 | — |
| Reactant | Diethylaminoethyl chloride | HCID 13364 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 9H-Fluorene-2,7-diol | HCID 14938383 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,7-Bis(2-diethylaminoethoxy)fluorene dihydrochloride | HCID 12445993 | — |
Reaction Steps
A solution of 2-diethylaminoethyl chloride [obtained from 12.9 g (0.075 mole) of 2-diethylaminoethyl chloride hydrochloride] in 100 ml of toluene (dried over molecular sieves) is added to a mixture of 4.9 g (0.025 mole) of 2,7-dihydroxyfluorene and 2.7 g (0.05 mole) of sodium methoxide in 200 ml of toluene (dried over molecular sieves). This mixture is refluxed with stirring for three hours. Upon cooling the mixture is filtered to remove the precipitated sodium chloride. The toluene solution is washed three times with water, then once with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. This mixture is filtered and the filtrate acidified to Congo Red with ethereal hydrogen chloride. The solid which precipitates is filtered, dissolved in butanone with enough methanol added to effect solution, decolorized with charcoal, and the product obtained at 80°C under vacuum, 2,7-bis(2-diethylaminoethoxy)fluorene dihydrochloride. M.P. 213°-216°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03947593 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-a68ca0459eb84c6498502e2289b5145e |
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| Source note | uspto-grants-1976_03 |
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