Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375737Generated: October 29, 2026

4-Nitrobenzyl chloroformate → HCID 54015813, compound

https://huagongshe.com/reaction/375737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl chloroformateHCID 78205—
Reactanttert-Butyl (3S)-3-hydroxybutanoateHCID 10154184—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 54015813HCID 5401581362.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3.84 g of tert-butyl (S)-3-hydroxybutyrate and 5.86 g of 4-dimethylaminopyridine in 20 ml of methylene chloride was added at 0° C. within 20 minutes a solution of 6.47 g of p-nitrobenzyl chloroformate in 20 ml of methylene chloride. The mixture was stirred for 3 hours at 0° C., then diluted with 50 ml of methylene chloride and washed successively with 1N hydrochloric acid, saturated sodium bicarbonate solution, and with brine. The organic layer was dried over sodium sulfate, and the solvent was evaporated in vacuo. The residual oil was chromatographed on silica gel using ethyl acetate/hexane (1:1, v/v) as eluent to yield 5.10 g of tert-butyl (S)-3-(4-nitrobenzyloxycarbonyloxy)-butyrate as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486466
Source datasetuspto-grants-1996_01
ORD IDord-e8e486a225e6400c9ff3ca67ee009af2
Source noteuspto-grants-1996_01