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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269594Generated: October 29, 2026

Potassium sodium tartarate → (2-(Benzyloxy)-5-iodophenyl)methanol

https://huagongshe.com/reaction/269594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
Reactant2-(Benzyloxy)-5-iodobenzaldehydeHCID 15043489—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
Product(2-(Benzyloxy)-5-iodophenyl)methanolHCID 59831381—

Reaction Conditions

Temperature0 °C

Reaction Steps

100 ml of a 1M diisobutylaluminum hydride solution in dichloromethane are added to a solution, cooled to 0° C., of 33.98 g (100.5 mmol) of 2-benzyloxy-5-iodobenzaldehyde (Example 2A) in 200 ml of dichloromethane. After stirring at 0° C. for 2 h, a saturated potassium sodium tartrate solution is added while cooling (highly exothermic reaction), and the reaction mixture is stirred for a further 2 h. After the separation of the phases, the organic phase is washed twice with water and once with a saturated aqueous sodium chloride solution and dried over sodium sulfate. The solvent is evaporated in vacuo. 31.8 g (93% of theory) of product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-7bcd6824560e4b9c9644522f7863956a
Source noteuspto-grants-2008_11