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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394659Generated: November 1, 2026

N-Iodosuccinimide → HCID 10927374, compound

https://huagongshe.com/reaction/1394659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant1-(2,2-Difluoroethoxy)-2,4-bis(1,1-dimethylethyl)benzeneHCID 17952768—
SolventDichloromethaneHCID 6344—
ProductHCID 10927374HCID 10927374100.1%

Reaction Conditions

Temperature38 °C

Reaction Steps

2,4-Di-tert-butyl-1-(2,2-difluoro-ethoxy)-benzene (6.75 g, 25 mmol), N-iodosuccinimide (6.74 g, 30 mmol) and p-toluenesulfonic acid monohydrate (1.90 g, 10 mmol) were combined in dichloromethane (75 mL) and heated at 38° C. for 7 h. TLC (hexanes) indicated a small amount of starting material still present and the reaction was treated with additional N-iodosuccinimde (0.33 g). After 4 h the reaction was washed with 10% Na2SO2O3 solution (50 mL). The aqueous was backwashed with dichloromethane (100 mL) and then the combined organic portions washed with water (75 mL) and the combined organic portions washed with water (100 mL), dried (MgSO4), filtered and evaporated in vacuo to provide an orange oil (9.92 g). The material was purified by flash chromatography using hexane to give 8.88 g (90%) of a light pink oil which solidified over time. 1H NMR (250 MHz, CDCl3): δ 7.66 (d, 1H, J=2.4), 7.36 (d, 1H, =2.4), 6.29 (tt, 1H, J=55.3, J=4.3), 4.24 (td, 2H, J=13.2, J=4.3), 1.40 (s, 9H), 1.29 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348359B2
Source datasetuspto-grants-2008_03
ORD IDord-52885482e1a34a3a8ae87b8aaab8e350
Source noteuspto-grants-2008_03