Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | HCID 56630527 | HCID 56630527 | — |
| Product | HCID 13398955 | HCID 13398955 | — |
Reaction Steps
211 g (1 mol) of 5-morpholinonon-4-ene were dissolved in 1 liter of tetrahydrofuran. First 129.5 g (1 mol) of amidosulfonyl chloride in 300 ml of tetrahydrofuran and then 101 g (1 mol) of triethylamine were added dropwise to the solution, cooled to -40° C. The mixture was left to warm up to 20° C. and the precipitated triethylammonium hydrochloride was filtered off. The solvent was then distilled off and the residue was stirred for one hour with a mixture of 1 liter of methylene chloride and 250 ml of 2N hydrochloric acid. The organic phase was separated off, dried with sodium sulfate and distilled. This gave 152.3 g (65% of theory) of a colorless oil of boiling point 135°-138° C. at 0.3 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04650902 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-cc9917c9d246422191b2ad63950ac1b9 |
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| Source note | uspto-grants-1987_03 |
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