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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222449Generated: October 29, 2026

Hydrochloric Acid → ethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoate

https://huagongshe.com/reaction/222449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantEthyl (4R)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoateHCID 57351319—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoateHCID 5789401198.8%

Reaction Steps

Under atmosphere of argon, to a solution of (4R)-5-hydroxy-4-t-butoxycarbonylaminopentanoic acid ethyl ester (15.0 g), triethylamine (32.0 mL) and dimethylsulfoxide (39 mL) in ethyl acetate (120 mL), a solution of sulfur trioxide pyridine complex (18.3 g) in mixed solvent ethyl acetate (30 mL) and dimethylsulfoxide (75 mL) was added at 0° C., and the mixture was stirred for 1 hour. The reaction mixture was added by water (5 mL) at 0° C. and was added by 1N hydrochloric acid (240 mL). Separated aqueous layer was extracted by ethyl acetate. The combined organic layer was washed with water and brine successively, dried over an anhydrous sodium sulfate, concentrated under reduced pressure to give the title compound (14.7 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207223B2
Source datasetuspto-grants-2012_06
ORD IDord-052e1632a2c44812bd295e9f2c245524
Source noteuspto-grants-2012_06