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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780805Generated: October 25, 2026

Sodium triacetoxyborohydride → HCID 54338209, compound

https://huagongshe.com/reaction/1780805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-amino-N-(2,3-dimethylphenyl)benzamideHCID 6456586—
ReactantN-Boc-S-trityl-(L)-cysteinalHCID 10388929—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 54338209HCID 54338209—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631280
Source datasetuspto-grants-1997_05
ORD IDord-62f6a466590c4ce697af1f2b5e7f422b
Source noteuspto-grants-1997_05