HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376821Generated: October 30, 2026
Ethanol → (-)-6-[(4-chlorophenyl)-hydrazinomethyl]-1-methyl-1H-benzotriazole (R)-alpha-hydroxybenzeneacetate
https://huagongshe.com/reaction/1376821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | (-)-Mandelic acid | HCID 11914 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+)-6-[(4-chlorophenyl)hydrazinomethyl]-1-methyl-1H-benzotriazole monohydrochloride | HCID 18924324 | — |
| Solvent | Water | HCID 962 | — |
| Product | (-)-6-[(4-chlorophenyl)-hydrazinomethyl]-1-methyl-1H-benzotriazole (R)-alpha-hydroxybenzeneacetate | HCID 131720170 | 163.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663354 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-f7f7b8330183457a990d40f34e8faddf |
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| Source note | uspto-grants-1997_09 |
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