Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Chloromethyl chloroformate | HCID 62754 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Chloromethyl isopropyl carbonate | HCID 14787051 | — |
Reaction Steps
1.32 g of isopropanol was added to 2.63 g of chloromethyl chloroformate, then 20 ml of ethyl ether was added and the mixture solution was cooled to 0° C. The solution of 1.659 g of pyridine in 10 ml of ethyl ether was added into the solution, and the mixture was reacted for 1 hour at that temperature, and then reacted at room temperature for 5 hours. The reaction was stopped, and the filtrate was washed respectively with diluted hydrochloric acid and water once. The organic phase was dried and concentrated to give crude 1-chloromethyl isopropyl carbonate, which was directly used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858651B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-9079756c35ee4048ba253be72ae9ea19 |
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| Source note | uspto-grants-2010_12 |
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