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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497947Generated: October 30, 2026

Tetrahydrofuran → 1,1-Dimethylethyl 4-[[2-(4-chlorophenyl)-4,4-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinecarboxylate

https://huagongshe.com/reaction/1497947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-Chlorophenyl)-4,4-dimethyl-1-cyclohexene-1-carboxaldehydeHCID 87279414—
SolventTolueneHCID 1140—
Product1,1-Dimethylethyl 4-[[2-(4-chlorophenyl)-4,4-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinecarboxylateHCID 66713018—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a 2 L three neck RB flask provided with a mechanical stirrer were charged a solution of 4′-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1′-biphenyl]-2-carbaldehyde (50.0 g) in toluene (250 mL), BOC-piperazine (48.2 g) and anhydrous THF (250 mL). The yellow solution was stirred at 20° C. for 5 min. Sodium triacetoxyborohydride (52.7 g) was added in portion (note: the internal temperature rose to ˜29.5° C. in 15 min cooling may be needed). The yellow mixture was stirred at ˜25° C. for NLT 4 hrs. A conversion of starting material to product of 99.5% was observed by HPLC after a 3 hour reaction time.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199992B2
Source datasetuspto-grants-2015_12
ORD IDord-9dff5b1875514bd0acd16cbf7374d590
Source noteuspto-grants-2015_12