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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265901Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 178453913, compound

https://huagongshe.com/reaction/2265901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(Piperazin-1-yl)-1,2-benzoxazoleHCID 13232475—
ReactantHCID 178453924HCID 178453924—
SolventDichloromethaneHCID 6344—
ProductHCID 178453913HCID 17845391364%

Reaction Steps

A mixture of 3-piperazin-1-yl-1,2-benzisoxazole (1 g, 4.92 mmol), trans-[4-(2-oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (Intermediate A) (1.3 g, 5.41 mmol), in dichloromethane (15 ml) was stirred for 15 minutes at room temperature and sodium triacetoxyborohydride (1.88 g, 8.86 mmol) was added slowly and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was extracted with saturated NaHCO3-solution and two times dichloromethane. The organic layers were dried over sodium sulfate, filtrated and concentrated to dryness. The crude product was purified with column chromatography on silica gel using heptane:ethyl acetate 80:20->10:90. The product fractions were concentrated to give 1.34 g (64% yield) of a white solid. MS (m/e): 429.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858630B2
Source datasetuspto-grants-2010_12
ORD IDord-a0d829c9ae874f3f95723a94f2f17bde
Source noteuspto-grants-2010_12