HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 22155484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 6-Ethoxy-N-methyl-1,3-benzothiazole-2-sulfonamide | HCID 23274675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22155484 | HCID 22155484 | 83% |
Reaction Steps
A one molar solution of boron tribromide in CH2Cl2 (21 mL) was cooled to -76° C. in a dry ice/acetone bath. N-Methyl-6-ethoxy-2-benzothiazole-sulfonamide (1, og.; 0.0037 mol) was added and the reaction stirred in the dry ice bath for four hours. The reaction was removed, stirred at room temperature for 18 hours, poured into a mixture of 25 mL of crushed ice/25 mL water and stirred for 30 minutes. The crude material was collected and purified by dissolving in 10% Na2CO3, filtered, anc precipitated with dilute acetic acid (1:1) to give 0.75g (83.0% yield) of pure product, m.p. 189°-190° C.; NMR(DMSO-d ) delta 8.5-8.0(m, 3H); 7.6(d, lH); 7.4-7.2 (q, lH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04975449 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-09de840ece6547e4a9c489f8ac7085ea |
| Source note | uspto-grants-1990_12 |