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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369167Generated: October 29, 2026

Trifluoroacetic anhydride → HCID 9900550, compound

https://huagongshe.com/reaction/1369167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 12040691HCID 12040691—
SolventDichloromethaneHCID 6344—
ProductHCID 9900550HCID 9900550—

Reaction Steps

O-Ethyl-N-trifluoroacetyl-L-tyrosine (XIII, Example 17, 1.52 g, 5 mmol) and ferric chloride (0.89 g, 5 mmol) are suspended in methylene chloride (36 mL). Trifluoroacetic anhydride (2.12 mL, 15 mmol) is added over 1 hr at 20-25°. The reaction is stirred for 1 hr and then quenched with water (36 mL). The organic layer is separated and mixed with methanol (7 mL). The mixture is cooled to −20° for 1 hr and then filtered to give the same title compound as EXAMPLE 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576769B2
Source datasetuspto-grants-2003_06
ORD IDord-541e3126c31e42babc1cb2297d8ca0a8
Source noteuspto-grants-2003_06