HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780805Generated: October 25, 2026
Sodium triacetoxyborohydride → HCID 54338209, compound
https://huagongshe.com/reaction/1780805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-amino-N-(2,3-dimethylphenyl)benzamide | HCID 6456586 | — |
| Reactant | N-Boc-S-trityl-(L)-cysteinal | HCID 10388929 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 54338209 | HCID 54338209 | — |
Reaction Steps
To a solution of 2 (0.28 g) in 12 mL of 1,2-dichloroethane at 0° C. was added sodium triacetoxyborohydride (0.36 g) and N-t-butyloxycarbonyl-S-(triphenyl- methyl)cysteinal (0.35 g). The cooling bath was removed and the mixture was stirred for 4 h at 20° C. The solution was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was extracted with 50 mL each of 2% potassium hydrogen sulfate, saturated sodium bicarbonate, saturated sodium chloride, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a foam. NMR (300 MHz, CDCl3) δ 8.17 (1H, b), 7.46-7.18 (15H, m), 6.60 (1H, m), 3.13(2H, m,), 2.45(3H, m), 2.30 (3H, s), 2.18 (3H, s), 1.42 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631280 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-62f6a466590c4ce697af1f2b5e7f422b |
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| Source note | uspto-grants-1997_05 |
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