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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367868Generated: November 3, 2026

Acetic Acid → HCID 66910044, compound

https://huagongshe.com/reaction/2367868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86609778HCID 86609778—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 66910044HCID 66910044—

Reaction Steps

9-Formyl-2,7-di(Boc-amino)fluorene (0.47 g, 1.1 mmol) was dissolved in anhydrous methanol (MeOH) (5 mL) under an argon atmosphere. NaBH4 (1.2 eq, 1.3 mmol, 0.05 g) was added and the reaction was stirred at room temperature for five hours. The reaction was diluted with deionized water and acidified to pH 5 with glacial acetic acid. The reaction was extracted with ethyl acetate (2×100 mL) and the organic layers were washed with saturated NaHCO3 (4×20 mL) and brine (3×20 mL). The organic layers were dried over MgSO4, filtered and evaporated. The crude product, orange solid, was purified by flash chromatography: silica gel 60 Å gradient elution 1-5% methanol in chloroform (alternative gradient elution with 15-20% ethyl acetate in dichloromethane, “DCM”). Product was a yellow solid (0.39, 83%). 1H-NMR (CD3OD): δ90 (ppm) 7.9 (s, 0.5H, NH urethane); 7.7 (s, 2H, Ar); 7.6 (d, 2H, Ar); 7.4 (d, 2H, Ar); 4.0 (m, 1H, CH); 3.9 (m, 2H, CH2); 1.6 (s, 18H, Boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703115B2
Source datasetuspto-grants-2014_04
ORD IDord-14bc00d41ae14453a213fe9ca07a8303
Source noteuspto-grants-2014_04