HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898929Generated: October 25, 2026
Ethyl Acetate → Methyl 2-({2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethyl}thio)benzoate
https://huagongshe.com/reaction/898929
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoic acid, 2-mercapto-, methyl ester | HCID 21009 | — |
| Reactant | Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetate | HCID 86600965 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-({2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethyl}thio)benzoate | HCID 69259277 | — |
Reaction Steps
Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetate (5.454 g, 17.347 mmol) was dissolved in acetonitrile (100 ml), methyl 2-mercaptobenzoate (3.502 g, 20.816 mmol) and dipotassium carbonate (4.795 g, 34.694 mmol) was added. The solution was stirred for 10 hours at 60° C. EtOAc (40 ml) was added and the organic phase was washed with two portions of brine (2×40 ml, aq). The organic layer was dried (MgSO4) and the solvent was removed by evaporation to give 6.931 g crude of methyl 2-({2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethyl}thio)benzoate. The crude was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351858B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-a683bfe9dc8244a3a7b20ca567be503e |
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| Source note | uspto-grants-2008_04 |
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