Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 14093551 | HCID 14093551 | — |
| Product | HCID 14093553 | HCID 14093553 | 91% |
Reaction Steps
The methyl 2-methoxymethyl-2-methyl-3-hydroxypropionate was added at from 15° to 20° C. to 438 g (3.68 mol) of thionyl chloride, the temperature was then raised to 60° C. and the mixture was stirred until the evolution of gas had ended. Excess thionyl chloride was distilled off, 0.2 g (0.0025 mol) of pyridine was added to the residue, and the temperature was raised to 135° C. After the evolution of SO2 had ended, distillation gave 317.0 g (1.76 mol) of methyl 2-methoxymethyl-2-methyl-3chloropropionate of boiling point 94° C. 35 mbar, corresponding to a 91% yield, based on methyl 2-methoxymethyl-2-methyl-3-hydroxypropionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837357 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-39ca00056cb94ebaa3e22d119db013fe |
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| Source note | uspto-grants-1989_06 |
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