HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731379Generated: October 30, 2026
Sodium triacetoxyborohydride → HCID 57671260, compound
https://huagongshe.com/reaction/731379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 57671255 | HCID 57671255 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57671260 | HCID 57671260 | 60.8% |
Reaction Steps
2-Isopropylamino-cyclopent-1-enecarboxylic acid ethyl ester (2.44 g, 12.38 mmol) was dissolved in glacial acetic acid (30 mL) and sodium triacetoxyborohydride (7.87 g, 37.13 mmol) was added at 0° C. The solution was allowed to warm to 25° C. and stirred for 3 h. The acetic acid was removed in vacuo and the residue was dissolved in dichloromethane. The solution was washed with saturated aqueous sodium bicarbonate solution followed by saturated aqueous brine solution. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford the desired product, 2-isopropylamino-cyclopentanecarboxylic acid ethyl ester (1.5 g, 7.53 mmol, 60.8%), as a yellowish oil. LC-MS (ESI) calcd for C11H21NO2 199.16, found 200.2 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582626B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-c35ab577e15e49f780874c5fec451455 |
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| Source note | uspto-grants-2009_09 |
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