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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511821Generated: October 29, 2026

Bicarbonate Ion → HCID 87457533, compound

https://huagongshe.com/reaction/511821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantPotassium BromideHCID 253877—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 67290476HCID 67290476—
CatalystCopper SulfateHCID 24462—
CatalystTempoHCID 2724126—
SolventDichloromethaneHCID 6344—
ProductHCID 87457533HCID 8745753388.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101616B2
Source datasetuspto-grants-2015_08
ORD IDord-89a2faa1a602480eb90831035c8f4a22
Source noteuspto-grants-2015_08