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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295630Generated: October 27, 2026

1,2-Dichloroethane → tert-butyl N-((2S)-1-oxopentan-2-yl)carbamate

https://huagongshe.com/reaction/1295630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTolueneHCID 1140—
ReactantDichloroacetic AcidHCID 6597—
Reactant(S)-tert-Butyl (1-hydroxypentan-2-yl)carbamateHCID 13969854—
SolventDimethyl SulfoxideHCID 679—
Producttert-butyl N-((2S)-1-oxopentan-2-yl)carbamateHCID 10262225—

Reaction Conditions

Temperature0 °C

Reaction Steps

To Boc-norvalinol (7.77 g, 38 mmol), in anhydrous dimethylsulfoxide (153 mL) and toluene (153 mL) was added EDC (73.32 g, 382 mmol). After the solution was cooled to 0° C., dichloroacetic acid (15.8 mL, 191 mmol) was added dropwise. After addition was complete, the reaction was stirred for 15 min. The solution was allowed to warm to room temperature over a period of 2 h. The reaction mixture was concentrated to remove the toluene, then dissolved in ethyl acetate. The solution was washed successively with 1N sodium bisulfate, saturated sodium bicarbonate and brine, dried over sodium sulfate, filtered and concentrated to afford crude Boc-norvalinal which was used directly in the next step. TLC Rf=0.84 (40% ethyl acetate/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244721B2
Source datasetuspto-grants-2007_07
ORD IDord-ddb558eb32a34dcdb6fe5403537c5ec6
Source noteuspto-grants-2007_07