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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802789Generated: November 1, 2026

Triethylamine → methanesulfonic acid 2-(2-isopropyl-2H-tetrazol-5-yl)-ethyl ester

https://huagongshe.com/reaction/1802789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2-isopropyl-2H-tetrazol-5-yl)-ethanolHCID 57899216—
Reactant2-(1-isopropyl-1H-tetrazol-5-yl)-ethanolHCID 57899222—
SolventDichloromethaneHCID 6344—
Productmethanesulfonic acid 2-(1-isopropyl-1H-tetrazol-5-yl)-ethyl esterHCID 578992504%
Productmethanesulfonic acid 2-(2-isopropyl-2H-tetrazol-5-yl)-ethyl esterHCID 5789930717%

Reaction Steps

To a mixture of 2(2-isopropyl-2H-tetrazol-5-yl)-ethanol and 2-(1-isopropyl-1H-tetrazol-5-yl)-ethanol (1.5 g, 9.6 mmol) in methylene chloride (40 mL) was added methanesulfonyl chloride (0.82 mL, 11 mmol) and triethylamine (2.67 mL, 19.2 mmol). The solution was stirred at room temperature for 6 h, loaded on to a silica gel column, and eluted using methylene chloride/heptane followed by ethyl acetate/methylene chloride to provide methanesulfonic acid 2(2-isopropyl-2H-tetrazol-5-yl)-ethyl ester (370 mg, 17% yield) and methanesulfonic acid 2(1-isopropyl-1H-tetrazol-5-yl)-ethyl ester (80 mg, 4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349883B2
Source datasetuspto-grants-2013_01
ORD IDord-8051bc2dcdde45b295a898fe66d72e87
Source noteuspto-grants-2013_01