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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620792Generated: October 25, 2026

Hydrochloric Acid → HCID 54137898, compound

https://huagongshe.com/reaction/620792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium ChlorideHCID 5234—
ReactantBromoacetic AcidHCID 6227—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-butyl (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 11078078—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 54137898HCID 5413789878.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (2S,4R)-4-t-butyldimethylsilyloxy-1-t-butoxycarbonyl-2-(hydroxymethyl)pyrrolidine (0.62 g), 2-bromoacetic acid (0.26 g), 85% potassium hydroxide (0.37 g), and potassium iodide (0.93 g) in t-butyl alcohol (12 ml) was heated at 50° C. for 3 hours. The mixture was poured into water (100 ml), adjusted to pH 4 with 1N hydrochloric acid and saturated with sodium chloride. The aqueous mixture was extracted with three 50 ml portions of ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (30 g ) eluting with a mixture of methanol and dichloromethane (1:9 V/V) to give (2S,4R)-1-t-butoxycarbonyl-4-t-butyldimethylsilyloxy-2-(carboxymethyloxymethyl)pyrrolidine (0.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822787
Source datasetuspto-grants-1989_04
ORD IDord-cca902987ef84e6990b3784a70923176
Source noteuspto-grants-1989_04