HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37043Generated: October 25, 2026
Sodium cyanoborohydride → 1,13-Bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane
https://huagongshe.com/reaction/37043
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-(Benzyloxy)propanal | HCID 10888261 | — |
| Reactant | 1,13-Bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane 1,5-Diamino-1,5-dibenzyloxymethyl-3-azapentane | HCID 86748684 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,13-Bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane | HCID 19438505 | — |
Reaction Steps
1,13-Bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane 1,5-Diamino-1,5-dibenzyloxymethyl-3-azapentane (0.50 g, 1.5 mmol) was dissolved in methanol (20 ml). 3-Benzyloxypropanal (0.50 q, 3 mmol), sodium cyanoborohydride (0.11 g, 3 mmol) and 3 Å molecular sieve (10 g) were added and the mixture was stirred for 16 hours at ambient temperature. The reaction mixture was filtered, water (20 ml) was added and the mixture was acidified with hydrochloric acid to pH 3. The mixture was extracted with diethyl ether (2×25 ml), the ether solution was dried with magnesium sulphate, the solution was evaporated and the mixture was chromatographed on silica. 1,13-Bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane was isolated as a white solid. Yield 0.40 g (42%), FAB MS: 640(M+1). The structure was confirmed by 1H NMR and 13C NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05419893 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-2369ec2926a24e8ebc8b3a6458ffae7e |
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| Source note | uspto-grants-1995_05 |
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