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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303970Generated: November 1, 2026

Hydrochloric Acid → HCID 17818832, compound

https://huagongshe.com/reaction/2303970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantSodium chloroacetateHCID 23665759—
ReactantHCID 70150758HCID 70150758—
SolventDimethyl SulfoxideHCID 679—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductHCID 17818832HCID 1781883274.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a DMSO (50 ml) suspension of 3.63 g (0.100 mol) of sodium hydride, a DMSO solution (30 ml) of 31.57 g (0.100 mol) of benzyl 3,4-dichlorophenylacetate was added at a temperature of 30° C. or below over a period of 45 minutes, and then the solution was further stirred at an internal temperature of 25° C. for 45 minutes. Then 11.65 g (0.100 mol) of sodium chloroacetate was added over a period of 10 minutes and the suspension was stirred at an internal temperature of 25° C. for 18.5 hours. The reaction solution was added dropwise into 50 ml of 2N hydrochloric acid and 250 ml of ice water while maintaining the internal temperature at 20° C. or below, and then 250 ml of ethyl acetate was added to the mixed solution. After separating the liquid, the organic layer was washed with 250 ml of water and then further washed with 250 ml of a 5% saline solution. It was then concentrated under reduced pressure, again concentrated under reduced pressure by adding 50 ml of toluene and further concentrated under reduced pressure by additionally adding 50 ml of toluene to obtain a crude product. Then 100 ml of toluene was added and the solution was heated to an internal temperature of 90° C. and stirred for one hour, after which 100 ml of heptane was added at an internal temperature of 80° C. and the solution was cooled slowly until the internal temperature dropped to 25° C. The precipitated crystals were filtered out and washed twice with 25 ml of heptane to obtain 26.40 g (74.7% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433174B1
Source datasetuspto-grants-2002_08
ORD IDord-ea8825ddcf5f4d449d737b4b87d23758
Source noteuspto-grants-2002_08