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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13977Generated: October 30, 2026

(+/-)-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl azide → (+/-)-1-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methanamine

https://huagongshe.com/reaction/13977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl azideHCID 86598581—
CatalystPlatinumHCID 23939—
Product(+/-)-1-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methanamineHCID 1137908977%

Reaction Steps

Treatment of (±)-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl 4-methylbenzenesulfonate (1.4 g, 3.70 mmol) with sodium azide (0.96 g, 14.78 mmol) generally according to the procedure described for Intermediate 24 gave (±)-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl azide as a crude oil. Treatment of the azide with sulfided platinum on carbon (5 wt. %, 0.15 g) generally according to the procedure described for Example 2 provided 0.74 g (77%) of (±)-1-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methanamine as a white solid, hydrochloride salt. mp 270° C. (dec); Anal. calcd. for C12H14ClNOHCl: C, 55.4; H, 5.81; N, 5.38. Found: C, 55.4; H, 5.8; N, 4.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728155B2
Source datasetuspto-grants-2010_06
ORD IDord-8013f3c6e53e4296bde256e5f84d842e
Source noteuspto-grants-2010_06