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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860867Generated: October 26, 2026

Sodium Hydroxide → (6-bromo-1-hydroxy-2,3-dihydro-1H-inden-2-yl)acetic Acid

https://huagongshe.com/reaction/860867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-boranyl-2-methylpropan-2-amineHCID 3639180—
Reactantethyl(6-bromo-1-oxo-2,3-dihydro-1H-inden-2-yl)acetateHCID 86592225—
SolventTetrahydrofuranHCID 8028—
Product(6-bromo-1-hydroxy-2,3-dihydro-1H-inden-2-yl)acetic AcidHCID 67104698—

Reaction Steps

The product from Example 52A in THF was treated with tert-butylaminoborane (1.18 g, 13.5 mmol) and heated at 40–45° C. for 2.5 hours. The mixture was treated with sodium hydroxide solution (1.8 g in water, 40 mL) and heating was continued for 30 minutes. The mixture was allowed to cool to room temperature and the aqueous layer was separated. The organic layer was diluted with isopropyl acetate (40 mL) and water (40 mL) and combined with the aqueous layer. The solution was cooled to 0° C. and the pH was adjusted to 2 by addition of concentrated hydrochloric acid. The mixture was filtered and the fitler cake dried at room temperature. The solid was slurried in dichloromethane (6 mL), refiltered, and redried to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153889B2
Source datasetuspto-grants-2006_12
ORD IDord-a66d7f584663449a91edaaace43693df
Source noteuspto-grants-2006_12