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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790808Generated: November 1, 2026

Trifluoroacetic acid → 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acid

https://huagongshe.com/reaction/1790808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantiodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acidHCID 23387399—
SolventDichloromethaneHCID 6344—
Product4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acidHCID 23387534—

Reaction Steps

To a solution of 4-methoxybenzyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) benzoate (10.2 g, 19.04 mmole) in dichloromethane (100 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred 3 hours at room temperature. The solution was evaporated under reduced pressure and co-evaporated two times with toluene. The product was isolated by silica gel column chromatography. Yield: 6.9 g=87%. The product may be activated and esterified direct to a drug or converted to iodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acid as described above, that is by treatment with a base, chloroiodomethane, separation and then treatment with NaI.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-61a76cca51a74f099b8435aaf4b84a1d
Source noteuspto-grants-2006_07