HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanesulfonyl chloride → Tert-butyl 2-(3-(1-methylethylsulfonamido)phenoxy)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanesulfonyl chloride | HCID 82408 | — |
| Reactant | tert-butyl N-[2-(3-aminophenoxy)ethyl]carbamate | HCID 11557882 | — |
| Product | Tert-butyl 2-(3-(1-methylethylsulfonamido)phenoxy)ethylcarbamate | HCID 68524470 | — |
Reaction Steps
Sulfonation of tert-butyl 2-(3-aminophenoxy)ethylcarbamate (3) using propane-2-sulfonyl chloride following the method described in Example 1 gave tert-butyl 2-(3-(1-methylethylsulfonamido)phenoxy)ethylcarbamate (7) as a light yellow oil. 1H NMR (400 MHz, DMSO-d6) δ 9.70 (s, 1H), 7.17 (t, J=8.0 Hz, 1H), 6.97 (t, J=6.0 Hz, 1H), 6.76-6.79 (m, 2H), 6.60-6.62 (m, 1H), 3.16-3.30 (m, 3H), 1.35 (s, 9H), 1.19 (d, J=6.8 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193669B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-360d0a2753a94e399cd17cf0c78a4a61 |
| Source note | uspto-grants-2015_11 |