HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274046Generated: October 27, 2026
Potassium Hydroxide → 2-(8-benzylamino-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yloxy)-2-methylpropionic acid
https://huagongshe.com/reaction/274046
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Propanol, 1,1,1-trichloro-2-methyl-, hydrate | HCID 12219832 | — |
| Reactant | HCID 18007284 | HCID 18007284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(8-benzylamino-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yloxy)-2-methylpropionic acid | HCID 20094737 | 39.8% |
Reaction Steps
To a mixture of 8-benzylamino-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ol (970 mg) and 1,1,1-trichloro-2-methyl-2-propanol hydrate (1.28 g) in acetone (30 ml) was added portionwise powder KOH (1.71 g) and the mixture was stirred for 20 hours at ambient temperature. After the solvent was evaporated in vacuo, the residue was poured into 1N sodium hydroxide (30 ml) and washed with diethyl ether. The pH of the aqueous layer was adjusted to 6.0 with 3N hydrochloric acid. The precipitates were filtered off. The filtrate was concentrated in vacuo and water was added to the residue. The resulting precipitates were collected by filtration and dried to give 2-[8-benzylamino-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yloxy]-2-methylpropionic acid (0.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387710 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-74828932c7fb4ca9b27ccec206303d0d |
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| Source note | uspto-grants-1995_02 |
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