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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288620Generated: October 31, 2026

Ethanol → (-)-6-[(4-chlorophenyl)-hydrazinomethyl]-1-methyl-1H-benzotriazole (R)-alpha-hydroxybenzeneacetate

https://huagongshe.com/reaction/1288620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(-)-Mandelic acidHCID 11914—
ReactantSodium HydroxideHCID 14798—
Reactant(+)-6-[(4-chlorophenyl)hydrazinomethyl]-1-methyl-1H-benzotriazole monohydrochlorideHCID 18924324—
SolventWaterHCID 962—
Product(-)-6-[(4-chlorophenyl)-hydrazinomethyl]-1-methyl-1H-benzotriazole (R)-alpha-hydroxybenzeneacetateHCID 131720170163.7%

Reaction Conditions

Temperature14 °C

Reaction Steps

To a mixture of 200 g of intermediate 2-a and 479 ml of ethanol at 23° C. was added a solution of 23.94 g of sodium hydroxide in 180 ml of water. After stirring for 10 min. there were added 50.2 g of (-)-(R)α-hydroxybenzeneacetic acid. The whole was stirred for 30 min. at 60° C. and the product was crystallized by adding some product crystals obtained in a previous low-scale set-up. Then the whole was stirred for 2 hours at 50° C. and overnight at room temperature. The reaction mixture was cooled (temp.14° C.) and stirred for 1 hour. The product was filtered off, washed with ethanol and dried in vacuo, yielding 118.8 g (87%) of (±)-6-[(4-chlorophenyl)-hydrazinomethyl]-1-methyl-1H-benzotriazole (R)-α-hydroxybenzeneacetate (1:1) monohydrate (interm. 3-a); diastereomeric excess: 92.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05746840
Source datasetuspto-grants-1998_05
ORD IDord-d8fced3eccc44705baa6b81d3d8251c0
Source noteuspto-grants-1998_05