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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57150Generated: October 27, 2026

(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester → (3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amine

https://huagongshe.com/reaction/57150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl esterHCID 57920462—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amineHCID 57920455—

Reaction Steps

A solution of compound 125-C (2.7 g, 6.9 mmol) in dichloromethane (40 mL) and trifluoroacetic acid (40 mL) was stirred at rt for 4 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate, and the solvent evaporated in vacuo to afford compound 125-D as a colorless solid (1.86 g, 93%). 1H-NMR (CDCl3): δ 2.16 (s, 3H), 4.37 (s, 2H), 7.09-7.32 (m, 5H), 7.40 (d, 1H), 7.60 (d, 1H); MS: m/z 290.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434711B2
Source datasetuspto-grants-2016_09
ORD IDord-5c9400fd974a4f1f90eb40d0012a7f7a
Source noteuspto-grants-2016_09