HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 23584604, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 1-Propanamine, 3-chloro-, hydrochloride | HCID 11469095 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23584604 | HCID 23584604 | 54.1% |
Reaction Steps
Tert-butyl alcohol (2.45 g, 33 mmol) was added to chlorosulfonyl isocyanate solution (4 g, 28.26 mmol) in CH2Cl2 (80 mL) at 0° C. and agitated for 30 min. Triethylamine (19.7 mL) and 3-chloropropylamine HCl (4.29 g, 33 mmol) were added to the mixture and agitated for 2 hr at room temperature, followed by extraction using CH2Cl2 and brine and drying over anhydrous MgSO4. The residue was purified by silica gel column chromatography to give tert-butyl N-(3-chloropropyl)sulfamoylcarbamate (2, 4.17 g, 54%). 1H NMR (300 MHz, CDCl3): δ 5.25 (br, 1H), 3.67-3.62 (m, 2H), 3.28-3.26 (m, 2H), 2.09-2.01 (m, 2H), 1.51 (S, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073906B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-9edf7ca8272946528c9814f298094ee2 |
| Source note | uspto-grants-2015_07 |