Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116123Generated: October 31, 2026

Sodium Azide → HCID 68963792, compound

https://huagongshe.com/reaction/2116123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAzideHCID 33558—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactantp-ToluenesulfonateHCID 85570—
ReactantBenzo[b]furan-2-boronic acidHCID 2776266—
Reactant(+/-)-(7-{[(Trifluoromethyl)sulfonyl]oxy}-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonateHCID 86599077—
ReactantHCID 86599195HCID 86599195—
ReactantHCID 86599196HCID 86599196—
CatalystPalladiumHCID 23938—
CatalystHCID 178418397HCID 178418397—
ProductHCID 68963792HCID 6896379234.3%

Reaction Steps

Treatment of (±)-(7-{[(trifluoromethyl)sulfonyl]oxy}-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate (1.5 g, 3.32 mmol) with 2-benzofuranboronic acid (0.81 g, 4.97 mmol), tetrakis(triphenylphosphine)palladium(0) (0.38 g, 0.33 mmol), and potassium phosphate (1.41 g, 6.63 mmol) generally according to the procedure described for Intermediate 50 provided (±)-2′,3′-dihydro-2,7′-bi-1-benzofuran-2′-ylmethyl 4-methylbenzenesulfonate. Treatment of the tosylate with sodium azide (0.09 g, 1.32 mmol) generally according to the procedure described for Intermediate 98 afforded (±)-2′-(azidomethyl)-2′,3′-dihydro-2,7′-bi-1-benzofuran. Treatment of the azide with palladium on carbon (0.03 g, 10 wt. %) generally according to the procedure described for Example 1 provided 0.12 g (12%) of (±)-1-(2′,3′-dihydro-2,7′-bi-1-benzofuran-2′-yl)methanamine as a white solid, hydrochloride salt. mp >220° C. (dec); Anal. calcd. for C19H17NOHCl.1.0H2O: C, 63.85; H, 5.67; N, 4.38. Found: C, 63.54; H, 5.1; N, 4.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-27e8d113a2434fec9048ae86e0d23dfc
Source noteuspto-grants-2008_10