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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113170Generated: October 29, 2026

2-tert-Butyl-5-hydroxy-2,3-dihydro-benzofuran-2-carboxylic acid methyl ester → (2R)-2-tert-Butyl-5-{3-[2-chloro-4-(2,2,2-trifluoro-ethyl)-phenoxy]-propoxy}-2,3-dihydro-benzofuran-2-carboxylic acid

https://huagongshe.com/reaction/2113170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-5-hydroxy-2,3-dihydro-benzofuran-2-carboxylic acid methyl esterHCID 11459363—
ReactantBenzene, 2-chloro-1-(3-iodopropoxy)-4-(2,2,2-trifluoroethyl)-HCID 69050445—
Product(2R)-2-tert-Butyl-5-{3-[2-chloro-4-(2,2,2-trifluoro-ethyl)-phenoxy]-propoxy}-2,3-dihydro-benzofuran-2-carboxylic acidHCID 57643419—

Reaction Steps

The title compound was prepared following the general procedure described in Example 1, Step 4, employing the chiral phenol prepared in step 1 and the iodide prepared in Example 14, Step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524882B2
Source datasetuspto-grants-2009_04
ORD IDord-4e22ef240be448e5a72ab665249a9b1f
Source noteuspto-grants-2009_04