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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221022Generated: October 26, 2026

2-((Phenylmethoxy)methyl)-5-(tributylstannyl)-2H-tetrazole → HCID 66607043, compound

https://huagongshe.com/reaction/221022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((Phenylmethoxy)methyl)-5-(tributylstannyl)-2H-tetrazoleHCID 11340561—
Reactant1-(2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl)-3-(5bromo-2-thienylmethyl)-4-chlorobenzeneHCID 60041289—
ProductHCID 66607043HCID 66607043—

Reaction Steps

1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-(5-bromo-2-thienylmethyl)-4-chlorobenzene obtained in Example 128-(4) and (2-benzyloxymethyl-2H-tetrazol-5-yl)trin-butyltin (see Tetrahedron Lett. (2000) 2805) were treated in a manner similar to Example 128-(5) to give 1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-(5-(2-benzyloxymethyl-2H-tetrazol-5-yl)-2-thienylmethyl)-4-chlorobenzene as colorless solid. APCI-Mass m/Z 727/729 (M+H). (2) A mixture of 1-(2,3,4,6-tetra-O-acetyl-β-Dglucopyranosyl)-3-(5-(2-benzyloxymethyl-2H-tetrazol-5-yl)-2-thienylmethyl)-4-chlorobenzene (247 mg), 6M aqueous hydrochloric acid solution (2 ml) and methanol (20 ml) was refluxed overnight. The solvent was evaporated under reduced pressure and the residue was triturated with diethyl ether to give the desired 1-(β-D-glucopyranosyl)-4-chloro-3-(5-(1H-tetrazol-5-yl)-2-thienylmethyl)benzene (172 mg) as colorless powder. ESI-Mass m/Z 437/439 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202984B2
Source datasetuspto-grants-2012_06
ORD IDord-3fa40cc1409e40c389d9783e1ce3920e
Source noteuspto-grants-2012_06