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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dichloroacetic Acid | HCID 6597 | — |
| Reactant | (S)-tert-Butyl (1-hydroxypentan-2-yl)carbamate | HCID 13969854 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | tert-butyl N-((2S)-1-oxopentan-2-yl)carbamate | HCID 10262225 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592316B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0a2beae3e1df40098ad56f2c0215fede |
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| Source note | uspto-grants-2009_09 |
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