Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402803Generated: October 27, 2026

Diisobutylaluminum hydride → 6-Chloro-2,2-dimethylchroman-8-carbaldehyde

https://huagongshe.com/reaction/402803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant6-Chloro-2,2-dimethyl-3,4-dihydro-2H-chromene-8-carboxylateHCID 86676815—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-Chloro-2,2-dimethylchroman-8-carbaldehydeHCID 77230853—

Reaction Conditions

Temperature-78 °C

Reaction Steps

6-Chloro-2,2-dimethyl-3,4-dihydro-2H-chromene-8-carboxylate (350 mg, 1.37 mmol) was dissolved in dichloromethane (6.87 mL) and cooled to −78° C. DIBAL-H (4.12 mL, 4.12 mmol) was added dropwise. The reaction mixture was warmed to room temperature and stirred for 1 hour. It was then cooled to 0° C., diluted with dichloromethane (10.0 mL) and water (2.00 mL) was added slowly, followed by a 15% aqueous NaOH solution (5.00 mL). The mixture was warmed to room temperature and stirred for 15 minutes. The organic layer was separated, dried over Na2SO4, filtered, and concentrated under vacuum. The crude alcohol was used directly in the next step without further purification. The crude alcohol was dissolved in dichloromethane (7.00 mL), and Dess-Martin periodinane (1.20 g, 2.75 mmol) was added in one portion at room temperature. The reaction mixture was stirred at room temperature for 30 minutes and then concentrated under vacuum on silica gel. It was then purified by silica gel chromatography eluting with 0-15% EtOAc/hexanes to give the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-eb00497ab7304ad08319006f22f0e54f
Source noteuspto-grants-2014_06