HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663616Generated: October 26, 2026
Chloroacetamide → tert-Butyl (2-chloroacetyl)carbamate
https://huagongshe.com/reaction/1663616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl alcohol 1,2-dichloroethane | HCID 21868497 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | tert-Butyl (2-chloroacetyl)carbamate | HCID 14221822 | 49% |
Reaction Steps
To a suspension of 2-chloroacetamide (25 g, 267 mmol) in 1,2-dichloroethane (125 mL) was added dropwise oxalyl chloride (28 mL, 321 mmol) at 0° C. After heating under reflux for 3 hr, the mixture was cooled to 0° C., tert-butyl alcohol/1,2-dichloroethane (75 mL, 1/1) was added to the mixture, and the mixture was stirred for 20 min. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with 1,2-dichloroethane. After washing with saturated aqueous sodium hydrogencarbonate solution and water, the extract was dried over anhydrous magnesium sulfate and filtrated. The solvent was evaporated under reduced pressure, and the residue was recrystallized from cyclohexane to give the title compound (25.6 g, 49%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034812B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-66eb0cd0199a43fea30fc799b7e2ad73 |
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| Source note | uspto-grants-2011_10 |
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