HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486167Generated: November 2, 2026
N-BOC-ethylenediamine → HCID 86722958, compound
https://huagongshe.com/reaction/1486167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86722957 | HCID 86722957 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86722958 | HCID 86722958 | — |
Reaction Steps
Titanium ethoxide (0.47 mL, 2.24 mmol) was added to a solution of (1-Hydroxy-4-oxo-cyclohexyl)-acetic acid benzyl ester (1.22 g, 4.65 mmol) and 2-(Boc-amino)ethylamine (0.97 g, 6.05 mmol) in DCM (5.0 mL) under argon. The reaction was stirred at RT for 5 hr. The reaction was concentrated in vacuo. The residue was diluted with methanol (23 mL) under argon and cooled to −78° C. Sodium triacetoxyborohydride (1.49 g, 7.03 mmol) was added in one portion and the reaction allowed to slowly warm to RT overnight. The reaction was quenched with 10% Na2CO3 and extracted with ethyl acetate (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated. The crude product was carried forward without purification. ESI-MS m/z 407 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422314B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-7d88bea5986c42d1999a46b338b18e95 |
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| Source note | uspto-grants-2016_08 |
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