HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607214Generated: October 29, 2026
Toluene → Methyl 2-methyl-2-mesyloxymethyl-3-(4-chlorophenyl)-3-keto-propanoate
https://huagongshe.com/reaction/1607214
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 2-methyl-2-hydroxymethyl-3-(4-chlorophenyl)-3-keto-propanoate | HCID 19852106 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-methyl-2-mesyloxymethyl-3-(4-chlorophenyl)-3-keto-propanoate | HCID 19852270 | 74% |
Reaction Steps
Into a 5 liter RBF is placed 100 g (4.37 mole) of methyl 2-methyl-2-hydroxymethyl-3-(4-chlorophenyl)-3-keto-propanoate, 473 g (4.25 mole) of triethylamine, and 2 liters of toluene. This mixture is cooled to -10° C. and methane sulfonyl chloride, 488 g (4.25 mole), is added over 30 minutes. The internal temperature rose to 40° C. by the end of the addition. After stirring at room temperature for 2 hours, the mixture is worked up with 4 liters of cold water and 1 liter methylene chloride. The resulting red semisolid (1400 g) is crystalized using 200 ml of hot ethyl acetate and adding 1500 ml of hexane. Yielding 1060 g (74%) of a light yellow solid mp 85°-86° C., methyl 2-methyl-2-mesyloxymethyl-3-(4-chlorophenyl)-3-keto-propanoate. NMR data was consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863947 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-103cee6d9c124303ae5524bc607ef47a |
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| Source note | uspto-grants-1989_09 |
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