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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860510Generated: November 3, 2026

Dibenzyl cyclohexane-1,1-dicarboxylate → HCID 18623884, compound

https://huagongshe.com/reaction/1860510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzyl cyclohexane-1,1-dicarboxylateHCID 15416540—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
ProductHCID 18623884HCID 1862388479.8%

Reaction Steps

A solution of dibenzyl cyclohexane-1,1-dicarboxylate (10.5 g, 30 mmol, from Step A) in 100 mL CH2Cl2 was cooled to −78° C. and a solution of diisobutylaluminum hydride (60 mL, 1 M in CH2Cl2, 60 mmol) was added dropwise. After 3.5 h the mixture was carefully quenched with sat'd ammonium chloride and 1 M HCl. The mixture was warmed to rt and poured into 200 mL water and 200 mmL CH2Cl2. The layers were separated and the aqueous layer was extracted with CH2Cl2. The combined organic layers were dried over magnesium sulfate and concentrated. Flash chromatography (400 g silica, 10/1 hexane/EtOAc) gave 5.9 g (79%) of the desired aldehyde. 1H NMR (500 MHz, CDCl3) δ1.4-1.6 (m, 16), 1.88-1.95 (m, 2H), 2.03-2.12 (m, 2H), 5.2 (s, 2H), 7.30-7.41 (m, 5H), 9.58 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531484B2
Source datasetuspto-grants-2003_03
ORD IDord-b251ce3f1d63443fb64d943db80be3e6
Source noteuspto-grants-2003_03