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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601605Generated: October 30, 2026

Benzaldehyde → HCID 59717847, compound

https://huagongshe.com/reaction/601605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58835358HCID 58835358—
SolventMethanolHCID 887—
ProductHCID 59717847HCID 5971784727.5%

Reaction Steps

Take up the mixture of 4-[4-(2-aminoethyl)phenoxy]benzenesulfonyl azide (0.210 g, 0.661 mmol) in methanol (9.9 mL). Add benzaldehyde (0.20 mL, 1.98 mmol) and 3 Å molecular sieves. Stir at room temperature overnight. Add NaBH4 (0.075 g, 1.98 mmol) and stir for 1.5 hours. Filter the reaction mixture and purify by flash 40 chromatography, eluting with 3% (2.0 M NH3 in methanol), 30% hexanes and 67% ethyl acetate to give the title compound (0.0696 g, 25.8%): TOF MS ES+383.1 (M+H)+, HRMS calcd for C21H23N2O3S 383.1429 (M+H)+. found 383.1436, time 0.33 min; TLC [silica gel 60 F254, 10% (2.0 M NH3 in methanol) in dichloromethane] Rf=0.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902372B2
Source datasetuspto-grants-2011_03
ORD IDord-cac1a7e7fb8c47bdb7a9589f01311281
Source noteuspto-grants-2011_03