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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840633Generated: October 31, 2026

Hydrochloric Acid → HCID 10554409, compound

https://huagongshe.com/reaction/840633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 54201845HCID 54201845—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10554409HCID 1055440947.5%

Reaction Conditions

Temperature-45 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (1.0 M, 1.68 mL, 1.68 mmol) was added dropwise into a cold (−78° C.) mixture of 2-[4′-(2-benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-2-methyl-3-phenyl-propionic acid ethyl ester (0.8 g, 1.68 mmol), and tetrahydrofuran (8.0 mL). The mixture was allowed to gradually warm up to −45° C., and stirred for 2 hours. Benzyl bromide (0.29 mL, 2.52 mmol) was added into the reaction mixture. The temperature was gradually raised to room temperature and the reaction was stirred for 15 hours. The mixture was then poured in to water, acidified with HCl (2 N) to pH=5, and extracted with ethyl acetate. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography on silica gel (hexanes/EtAOc 5:1) gave an clear oil (0.43 g). The product was saponified according to Example 1 step h, to give a white solid (0.32 g, 34% yield for two steps): MS m/e 538 (M+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369072B2
Source datasetuspto-grants-2002_04
ORD IDord-8fd0c8df054e4c9394fbf66e0d2b9b78
Source noteuspto-grants-2002_04