Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-[4-(chlorosulfonyl)phenyl]acetate | HCID 23388822 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 559409 | HCID 559409 | 62.3% |
Reaction Steps
Methyl 2-(4-chlorosulfonylphenyl)acetate (2.0 g, 8.04 mmol) was taken in dry DCM (50 mL) under argon atmosphere and cooled to 0-5° C., morpholine (0.77 mL, 8.84 mmol) followed by triethylamine (1.16 mL, 8.84 mmol) was added dropwise to the mixture at 0-5° C. Reaction mixture was then brought to room temperature and stirred for additional 2 hours. Reaction mixture was washed with water followed by brine solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product, which was purified by column chromatography using 14-20% ethyl acetate in hexane as eluent to give Methyl 2-(4-morpholinosulfonylphenyl)acetate (1.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340506B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-70ee2080e4ea40f0aace94ebd97e195a |
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| Source note | uspto-grants-2016_05 |
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