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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357790Generated: November 1, 2026

Lithium hydroxide, monohydrate → 1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl ester

https://huagongshe.com/reaction/1357790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 3-benzyl ester 2-tert-butyl esterHCID 15550522—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl esterHCID 15550523—

Reaction Steps

1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 3-benzyl ester 2-tert-butyl ester (6 g, 12 mmol) is dissolved in a mixture of 120 ml Tetrahydrofuran and 78 ml Water. LiOH·H2O (1 g, 24 mmol) is added. After 45 min., more Water (15 ml) is added and the reaction solution is stirred at room temp. for 24 h. The solvent is evaporated and the remaining solid is resolved in Water/Diethylether. The water layer is acidified to pH 1. The organic phase is separated and the water phase is extracted twice with Ethylacetate. The combined organic fractions are dried with MgSO4 and filtered. The solvent is evaporated to afford the product: Cal. 412.5, found (M)+ 412.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593351B2
Source datasetuspto-grants-2003_07
ORD IDord-f111ddaacc434ce5b88f8728035c8f12
Source noteuspto-grants-2003_07