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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860958Generated: November 3, 2026

Trifluoroborane-methyl sulfide → N-[3,5-dichloro-4-(2-bromo-4-hydroxy-5-isopropylphenoxy)benzoyl]glycine

https://huagongshe.com/reaction/860958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
Reactantmethyl-N-[3,5-dichloro-4-(2-bromo-4-methoxy-5-isopropylphenoxy)benzoyl]glycineHCID 69384859—
SolventDichloromethaneHCID 6344—
ProductN-[3,5-dichloro-4-(2-bromo-4-hydroxy-5-isopropylphenoxy)benzoyl]glycineHCID 1002799394.3%

Reaction Steps

Boron trifluoride dimethyl sulfide (10 μL, 80 μmol) was added at room temperature to a stirred solution of methyl-N-[3,5-dichloro-4-(2-bromo-4-methoxy-5-isopropylphenoxy)benzoyl]glycine (1.0 mg, 2.0 μmol) and dichloromethane (0.50 mL). The reaction mixture was stirred at room temperature for 8 hours and then treated with ice-water, extracted with ethyl acetate and washed with water. The organic phase was dried over sodium sulphate and concentrated to give a light yellow solid. The solid was purified on column (MPLC, silica gel, chloroform/methanol/acetic acid, gradient elution from 1/0/0 to 95/5/0.5) to give 0.90 mg (94%) of N-[3,5-dichloro-4-(2-bromo-4-hydroxy-5-isopropylphenoxy)benzoyl]glycine. LC-MS (ES−1): m/z 476.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153997B2
Source datasetuspto-grants-2006_12
ORD IDord-83c5f8f9df0f407991abbe39700853e7
Source noteuspto-grants-2006_12