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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276046Generated: November 1, 2026

Toluene → HCID 89996173, compound

https://huagongshe.com/reaction/2276046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 131733426HCID 131733426—
SolventDichloromethaneHCID 6344—
ProductHCID 89996173HCID 8999617357.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the stirred solution of 1-tert-butyl 2′-ethyl-7′H-spiro[azetidine-3,5′-furo[3,4-b]pyridine]-1,2′-dicarboxylate (0.5 g, 1.5 mmol, 1 eq.) in DCM (18 mL) at −78° C. under nitrogen atmosphere was added 25% DIBAL-H in toluene (0.64 g, 2.6 mL, 4.5 mmol, 3 eq.). Resulting reaction mixture was stirred at −78° C. for 1 hour under nitrogen atmosphere. After complete consumption of starting material, reaction mixture was quenched by methanol (1.5 mL) followed by addition of saturated solution of sodium potassium tartarate salt (10 mL) at −78° C. and extracted with DCM (3×75 mL). Combined organic layer was dried over sodium sulphate, concentrated under reduced pressure to afford the title compound as brown solid (0.25 g, crude). Crude compound was used as such for the next reaction. LC-MS (m/z): 291.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09131697B2
Source datasetuspto-grants-2015_09
ORD IDord-16d5bfb8848b43218a1fc02e8f4db262
Source noteuspto-grants-2015_09