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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519640Generated: November 2, 2026

Sodium triacetoxyborohydride → HCID 86694486, compound

https://huagongshe.com/reaction/1519640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67513243HCID 67513243—
Reactant2-(1-Oxo-1,3-dihydroisobenzofuran-5-yl)acetaldehydeHCID 77231261—
SolventDichloromethaneHCID 6344—
ProductHCID 86694486HCID 86694486—

Reaction Steps

A solution of crude 2-(difluoromethoxy)-4-(2-piperazin-1-ylethyl)benzonitrile (15 mg, 0.05 mmol), (1-oxo-1,3-dihydro-2-benzofuran-5-yl)acetaldehyde (18 mg, 0.1 mmol) and NaBH(OAc)3 (100 mg, 0.47 mmol) in 10 mL of anhydrous DCM was stirred at ambient temperature overnight. The reaction mixture was added 50 mL of DCM, washed with brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified with prep-TLC to afford 2-(difluoromethoxy)-4-(2-{4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrile. 1H-NMR (400 MHz, CDCl3) δ 7.82 (d, J=7.8 Hz, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.33˜7.36 (m, 2H), 7.13˜7.20 (m, 2H), 6.33 (t, J=71.2 Hz, 1H), 5.26 (s, 2H), 2.99˜3.08 (m, 2H), 2.87˜2.90 (m, 2H), 2.62˜2.84 (m, 12H). (0.15 μm)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073882B2
Source datasetuspto-grants-2015_07
ORD IDord-d349c1c0c5714818a4230557993b0308
Source noteuspto-grants-2015_07