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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173429Generated: October 31, 2026

Tetrahydrofuran → HCID 67517692, compound

https://huagongshe.com/reaction/2173429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant1-(1,1-Dimethylethyl) 4-(9H-fluoren-9-ylmethyl) 2-oxo-1,4-piperazinedicarboxylateHCID 89754486—
SolventDichloromethaneHCID 6344—
ProductHCID 67517692HCID 67517692—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a pre-dried RB flask, 1-tert-butyl 4-(9H-fluoren-9-ylmethyl) 2-oxopiperazine-1,4-dicarboxylate (6.5 g, 15.39 mmol) was dissolved in CH2Cl2 (150 mL) and THF (15 mL) under N2 and was cooled down to −78° C. DIBAL-H (23.08 mL, 23.08 mmol) was added slowly. Let reaction stir at −78° C. for 2 hours. Then saturated Rochelle's salt water solution (150 mL) was added to quenched reaction. Reaction was slowly warmed up to room temperature. Then it was passed through a Celite® pad. Filtering pad was washed with ether (100 mL×2). Then layers were separated and aq. layer was extracted with 50 mL of EtOAc twice. Organic phases were combined and were washed with water and brine (50 mL) respectively. Then it was passed anhydrous Na2SO4. Concentration gave crude product as white solid that was used directly in next step. LC/MS: (M+23)+=447.16

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-0133e27cb6cd49ef8490600b0e3f9046
Source noteuspto-grants-2015_06