Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59651Generated: October 27, 2026

Formic Acid → Tert-butyl N-[(Benzenesulfonyl)(2-bromo-4-cyanophenyl)methyl]carbamate

https://huagongshe.com/reaction/59651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTetrahydrofuranHCID 8028—
ReactantBenzenesulfinic acid, sodium saltHCID 2723840—
Reactant3-Bromo-4-formylbenzonitrileHCID 20510518—
ReactantTert-butylcarbamateHCID 21252905—
SolventWaterHCID 962—
ProductTert-butyl N-[(Benzenesulfonyl)(2-bromo-4-cyanophenyl)methyl]carbamateHCID 118691238—

Reaction Steps

3-Bromo-4-formyl-benzonitrile (20.5 g, 97.7 mmol), benzenesulfinic acid sodium salt (16.03 g, 97.6 mmol) and tert-butylcarbamate (11.4 g, 97.7 mmol) are suspended in water (312 mL) and THF (78 mL). Formic acid (28.8 g, 625 mmol) is added and the solution is stirred at room temperature for 6 days. Water (300 mL) is added and the precipitate is filtered off, washed with water and dried. The crude product is further purified by precipitation from tert-butylmethylether. Yield: 26.8 g; ESI mass spectrum: [M+Na]+=473 (bromine isotope pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440930B2
Source datasetuspto-grants-2016_09
ORD IDord-3e802816fb3946918173d636cb788fa2
Source noteuspto-grants-2016_09