HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709852Generated: November 1, 2026
Water → α,α-Bis(4-chlorophenyl)-4-piperidinemethanol
https://huagongshe.com/reaction/1709852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14698740 | HCID 14698740 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | α,α-Bis(4-chlorophenyl)-4-piperidinemethanol | HCID 14698743 | 35% |
Reaction Steps
To a slurry of 8.5 g (0.225 mole) of lithium aluminum hydride in 400 ml of anhydrous tetrahydrofuran was added a solution of 39.2 g (0.09 mole) of 4-[bis(4-chlorophenyl)hydroxymethyl]-N,N-diethyl-1-piperidinecarboxamide in 400 ml of tetrahydrofuran in a stream over a 15 min period. The mixture was heated at reflux for 24 hr, cooled, and treated successively with 8.5 ml of water, 25 ml of a 3N sodium hydroxide solution and 8.5 ml of water. The mixture was stirred for 0.5 hr and then filtered. The filtrate was concentrated under reduced pressure to give a gum which crystallized. The solid was triturated with petroleum ether (30°-60° C.), collected by filtration and recrystallized from benzene to yield 10.5 g (35%) of title compound as a white solid. An analytical sample was recrystallized from 2-propanol, mp 184°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950674 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-e38d8574482f44a5ae2e23ef1b39c5d5 |
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| Source note | uspto-grants-1990_08 |
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