HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511821Generated: October 29, 2026
Bicarbonate Ion → HCID 87457533, compound
https://huagongshe.com/reaction/511821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | HCID 67290476 | HCID 67290476 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Catalyst | Tempo | HCID 2724126 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87457533 | HCID 87457533 | 88.4% |
Reaction Steps
To a solution of (5-(cyclopropylmethoxy)pyridin-2-yl)methanol (4.5 g, 25 mmol) in dichloromethane (50 ml), was added a 15% potassium bromide aqueous solution (20 mL) followed by a saturated bicarbonate solution (20 ml). The biphasic mixture was cooled in an ice bath and TEMPO (200 mg, 1.3 mmol) was added. After stirring for 10 min, 5% sodium hypochlorite (30 ml) was dropwised. The reaction mixture was stirred for 10 min. The solution was poured into a separatory funnel and the organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was dissolved in dichloromethane (50 mL). Copper(II) sulfate (10.1 g, 63 mmol) followed by (R)-(+)-2-methyl-2-propanesulfinamide (3.1 g, 25 mmol) were added to the mixture respectively and the mixture was stirred for 18 hours at room temperature. The reaction mixture was filtrated off and the filtrate was concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (1:1 (v/v)) to give 6.2 g (87% yield) of the title compound as a flaky solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09101616B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-89a2faa1a602480eb90831035c8f4a22 |
|---|
| Source note | uspto-grants-2015_08 |
|---|