Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 18328605 | HCID 18328605 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 73437352 | HCID 73437352 | — |
Reaction Steps
Into a dried 1L 3 neck round bottom flask fitted with a nitrogen inlet, dropping funnel, thermometer, mechanical stirring and nitrogen outlet is added chloroform (300 ml) and 7-methylundecanol (93 g, 0.5 mol). Chlorosulfonic acid (60 g, 0.509 mol) is slowly added to the stirred mixture while maintaining 25-30° C. temperature with a ice bath. Once HCl evolution has stopped (1 hr.) slowly add sodium methoxide (25% in methanol) while keeping temperature at 25-30° C. until an aliquot at 5% concentration in water maintains a pH of 10.5. To the mixture is added hot ethanol (55° C., 2L). The mixture is vacuum filtered immediately. The filtrate is concentrated to a slurry on a rotary evaporator, cooled and then poured into 2L of ethyl ether. The mixture is chilled to 5° C., at which point crystallization occurs, and vacuum filtered. The crystals are dried in a vacuum oven at 50C for 3 hrs. to obtain a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06228829B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-f52a2b19fe1745a09875a9cb452daef0 |
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| Source note | uspto-grants-2001_05 |
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