HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508394Generated: October 28, 2026
Ethyl chloroformate → Ethyl hydrogen (1-hydroxy-2-methylpropan-2-yl)carbonimidate
https://huagongshe.com/reaction/508394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl hydrogen (1-hydroxy-2-methylpropan-2-yl)carbonimidate | HCID 235908 | — |
Reaction Steps
To a stirred solution of ethyl chloroformate (3 g, 0.027 mol.) and N-hydroxysuccinimide (3.8 g, 0.033 mol.) in 10 mL of DCM at 0° C. under nitrogen atmosphere was added N,N-Diisopropylethylamine (7.0 mL, 0.04 mol). The progress of the reaction was monitored by thin layer chromatography (TLC). After stirring for 3 hrs at room temperature. DCM was evaporated and the residue was dissolved in 10 mL of acetonitrile, cooled in an ice-bath and then added dropwise a solution of 2-amino-2-methyl-1-propanol (3.1 mL, 1.2 eq). The resulting mixture was stirred at ice-bath temperature for 1 h and then overnight at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). The reaction mixture was filtered, and the precipitate was washed with 2×10 mL DCM and dried over sodium sulfate. After removing the solvent under reduce pressure, the residue was purified by silica gel column chromatography to give ethyl (1-hydroxy-2-methylpropan-2-yl)carbamate as a colorless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096515B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-01024e8dab04447f8dd1220d5c5ed0b9 |
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| Source note | uspto-grants-2015_08 |
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