HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzenesulfonyl chloride → HCID 59054458, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | HCID 59054575 | HCID 59054575 | — |
| Product | HCID 59054458 | HCID 59054458 | — |
Reaction Steps
Following 17a synthetic method, using 4-fluorobenzenesulfonyl chloride (214.08 mg, 1.1 mmol) instead of 2-fluorobenzenesulfonyl chloride gave the final compound 19a; as a colorless oil; (93.99 mg, 55.4%). [α]D25: +12.8 (c=0.26, CHCl3); 1H-NMR (300 MHz, CDCl3): δ 7.77-7.73 (m, 2H), 7.24-7.21 (m, 7H), 6.92 (d, J=9 Hz, 1H), 4.21-4.14 (m, 1H), 3.15-2.90 (m, 2H); 13C NMR (300 MHz, acetone-d6): δ 171.55, 166.28, 162.95, 137.53, 136.53, 129.74, 129.62, 129.39, 128.24, 126.68, 115.93, 115.63, 57.29, 38.49; HRMS (ESI): calcd for: C15H14FNO4S [M+Na]+=346.0520, obsd [M+Na]+=346.0513.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409880B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-4eb8e4a8aa20448f929044fa20274fb2 |
| Source note | uspto-grants-2016_08 |