HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561313Generated: October 28, 2026
Chlorosulfonic acid → HCID 55279082, compound
https://huagongshe.com/reaction/561313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 5-Fluoro-1,2,3,4-tetrahydronaphthalene | HCID 579020 | — |
| Reactant | 4-fluoronaphthalene-1-sulfonyl Chloride | HCID 2774647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 55279082 | HCID 55279082 | — |
Reaction Steps
The compound was prepared according to Scheme 10 in a similar manner to the method for preparing 4-fluoro-naphthalene-1-sulfonyl chloride. Chlorosulfonic acid (2.65 g, 1.5 mL, 22.7 mmol) was stirred in a round-bottom flask cooled by a water bath at room temperature. 5-Fluoro-1,2,3,4-tetrahydro-naphthalene (0.62 g, 4.13 mmol) was added dropwise and the dark mixture was stirred for 30 minutes until gas evolution ceased. The reaction mixture was poured carefully over a mixture of ice (75 g) and dichloromethane (100 mL) and charged to a separatory funnel. The organic layer was separated, washed with brine and dried over MgSO4. Filtration and concentration in vacuo afforded a tan solid. Wt.: 860 mg (86%). 1H NMR (300 MHz, CDCl3) δ 7.97 (dd, 1H), 7.02 (t, 1H), 3.27 (m, 2H), 2.80 (m, 2H), 1.86 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063222B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-b6efb67d8eb94fa8bafe4fe312397c58 |
|---|
| Source note | uspto-grants-2011_11 |
|---|