Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Isohexane ethyl acetate | HCID 21882781 | 100% |
Reaction Steps
A solution of the sulfinamide from Step 5 (0.78 g, 1.63 mmol) and 1M HCl in diethyl ether (4 mL) in methanol (10 mL) was stirred at rt for 25 h. The solution was poured into sat. aq. sodium hydrogencarbonate (100 mL) and extracted with ethyl acetate (2×50 mL). The extracts were washed with water (50 mL), brine (20 mL), dried over sodium sulfate and concentrated to give a gum. The material was redissolved in pyridine (10 mL) and dichloromethane (10 mL) and stirred at 0° C. 2-Chloroethanesulfonyl chloride (0.2 mL, 1.0 mmol) was added dropwise. After stirring at rt for 18 h the mixture was diluted with 1M citric acid (100 mL) and extracted with dichloromethane-methanol (9:1, 2×100 mL). The extracts were washed with water (50 mL) and brine (20 mL, dried over sodium sulfate and concentrated. Chromatography, eluting with 50% then 100% ethyl acetate-isohexane, gave the sulfonamide as a pink solid (0.349 g, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435748B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-9a2af6a848714def84f2591207c140a7 |
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| Source note | uspto-grants-2008_10 |
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