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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307594Generated: October 27, 2026

Sodium Iodoacetate → 2-[[(4S,5R)-5-(1,2-dihydroxypropyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy]ethanoic acid, methyl ester

https://huagongshe.com/reaction/2307594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodoacetateHCID 5239—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Hydroxymethyl)-5-(1,2-dihydroxypropyl)-2,2-dimethyl-1,3-dioxolaneHCID 22607886—
SolventWaterHCID 962—
Product2-[[(4S,5R)-5-(1,2-dihydroxypropyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy]ethanoic acid, methyl esterHCID 8658876921.8%

Reaction Steps

A solution of 4-(hydroxymethyl)-5-(1,2-dihydroxypropyl)-2,2-dimethyl-1,3-dioxolane (63 g, 0.33 mol) and sodium iodoacetate (75 g, 0.36 mol) in water was treated with solid sodium hydroxide (16 g, 0.35 mol). The reaction mixture was stirred overnight and then washed with ethyl acetate and ether. The aqueous layer was concentrated. The resulting residue was dissolved in DMF (20 mL) and treated with iodomethane (37 mL, 0.6 mol). The resulting reaction mixture was stirred overnight. The reaction mixture was diluted with two volumes of salt water and extracted with ethyl acetate (6×). The combined organic layers were dried, and concentrated.to give 20 g of 2-[[(4S,5R)-5-(1,2-dihydroxypropyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy]ethanoic acid, methyl ester, a compound of formula (L), as a colorless viscous oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831186B2
Source datasetuspto-grants-2004_12
ORD IDord-26001097ed024701a0cf42d204d703a3
Source noteuspto-grants-2004_12