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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734204Generated: October 27, 2026

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

https://huagongshe.com/reaction/734204

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 washed successively with 1 N 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 numberUS07592316B2
Source datasetuspto-grants-2009_09
ORD IDord-0a2beae3e1df40098ad56f2c0215fede
Source noteuspto-grants-2009_09