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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778581Generated: November 2, 2026

Acetic Acid → HCID 131734838, compound

https://huagongshe.com/reaction/1778581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,4-DichlorobenzaldehydeHCID 22710—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 131734837HCID 131734837—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 131734838HCID 131734838—

Reaction Steps

A solution of 2-acetamido-2-{(1R,5S)-8-azabicyclo[3.2.1]octan-3-yl}-N-tert-butyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-hexanamide (170 mg, 0.37 mmol) and 3,4-dichlorobenzaldehyde (129 mg, 0.74 mmol) and acetic acid (44 mg, 41 μL, 0.74 mmol) in 1,2-dichloroethane (1 mL) was stirred at room temperature for 30 minutes then treated with sodium triacetoxyborohydride (196 mg, 0.93 mmol). After 24 hours, the reaction mixture was quenched with saturated aqueous sodium bicarbonate (10 mL), diluted with saturated aqueous sodium chloride (20 mL) and extracted with dichloromethane (3×20 mL). The combined organic phase was collected, dried over MgSO4, filtered and concentrated to give 2-acetamido-N-tert-butyl-2-{(1R,5S)-8-(3,4-dichlorobenzyl)-8-azabicyclo[3.2.1]octan-3-yl}-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-hexanamide as a pale yellow oil which was used immediately in the next step; m/z for C32H50BCl2N3O4 expected 621.3. found 644.5 (M+Na(35Cl))+, 622.1 (M+H(35Cl))+,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266908B2
Source datasetuspto-grants-2016_02
ORD IDord-cc09333f65cf4b8dba833bf9660a7728
Source noteuspto-grants-2016_02