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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290158Generated: November 2, 2026

9-Iodo-9-borabicyclo(3.3.1)nonane → 7-t-Butyl-5-[isopropyl-(4-hydroxy-phenyl)-amino]-3,3,6-trimethyl-2,3-dihydro-benzofuran

https://huagongshe.com/reaction/2290158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Iodo-9-borabicyclo(3.3.1)nonaneHCID 578231—
Reactant7-t-Butyl-5-[isopropyl-(4-methoxy-phenyl)-amino]-3,3,6-trimethyl-2,3-dihydro-benzofuranHCID 18699184—
SolventDichloromethaneHCID 6344—
SolventPentaneHCID 8003—
Product7-t-Butyl-5-[isopropyl-(4-hydroxy-phenyl)-amino]-3,3,6-trimethyl-2,3-dihydro-benzofuranHCID 18699173131.1%

Reaction Steps

Following general procedure M and using 7-t-butyl-5-[isopropyl-(4-methoxy-phenyl)-amino]-3,3,6-trimethyl-2,3-dihydro-benzofuran (Compound 57, 0.032 g, 0.083 mmol) and 1M solution of 9-iodo-9-borabicyclo[3.3.1]nonane (B-iodo-9-BBN) in hexanes (0.2 mL, 0.2 mmol) in 0.6 mL of anhydrous dichloromethane and 1 mL of n-pentane, the title compound (0.04 g) was obtained as a brown oil that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093838
Source datasetuspto-grants-2000_07
ORD IDord-34a4d56495b544debbb42daaf61dee4a
Source noteuspto-grants-2000_07