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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350469Generated: November 1, 2026

Trifluoroacetic acid → HCID 23512193, compound

https://huagongshe.com/reaction/350469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 4-(1-(tert-butoxycarbonyl)-4-(2,4-difluorophenoxy)-2-pyrrolidinyl methoxy]benzoateHCID 69333033—
SolventDichloromethaneHCID 6344—
ProductHCID 23512193HCID 2351219392.1%

Reaction Steps

To a stirred solution of methyl 4-[1-(tert-butoxycarbonyl)-4-(2,4-difluorophenoxy)-2-pyrrolidinyl methoxy]benzoate (529 mg, 1.15 mmol) in CH2Cl2 (5 ml) was added TFA (5 ml). The mixture was stirred overnight. The mixture was concentrated in vacuo and the residue was made basic by the addition of sat. NaHCO3. The mixture was extracted with CHCl3 (2×100 ml). The extracts were dried over K2CO3 and evaporated to give methyl 4-[4-(2,4-difluorophenoxy)-2-pyrrolidinyl methoxy]benzoate (385 mg, 92%) as a yellow oil. 1H-NMR (CDCl3) δ 1.89–1.95 (m, 1 H), 2.28–2.35 (m, 1 H), 3.09 (dd, J=12.5, 4.9 Hz, 1 H), 3.33 (d, J=12.5 Hz, 1 H), 3.60 (m, 1 H), 3.86 (s, 3 H), 4.10 (d, J=5.6 Hz, 2H), 4.84(m, 1H), 6.73–6.89(m, 3 H), 6.91 (d, J=8.5 Hz, 2H), 7.96 (d, J=8.5 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-df6e7d85c4c745528ccef8d48614e2c0
Source noteuspto-grants-2007_02