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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684814Generated: October 27, 2026

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

https://huagongshe.com/reaction/1684814

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 numberUSRE043298E1
Source datasetuspto-grants-2012_04
ORD IDord-35d18a1a962e4b69bdc1de88b9381d92
Source noteuspto-grants-2012_04