Trifluoroacetic acid → (2-Ethoxy-5-oxo-tetrahydrofuran-3-yl)-carbamic acid allyl ester

HRID 1824435Notes

Reaction equation

HRID 1824435 reaction equation
C(O[C:6](=[O:23])[CH2:7][CH:8]([NH:16][C:17]([O:19][CH2:20][CH:21]=[CH2:22])=[O:18])[CH:9]([O:13]CC)[O:10][CH2:11][CH3:12])(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:20]([O:19][C:17](=[O:18])[NH:16][CH:8]1[CH2:7][C:6](=[O:23])[O:13][CH:9]1[O:10][CH2:11][CH3:12])[CH:21]=[CH2:22]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 235987123-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl ester

Product 1

HCID 22149038(2-Ethoxy-5-oxo-tetrahydrofuran-3-yl)-carbamic acid allyl esterYield 85%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A solution of the crude 3-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl ester, 103, obtained in the procedure above, in CH2Cl2 (50 mL) is treated with triflouroacetic acid (50 mL). After the consumption of starting material, the organics are reduced under vacuum. The residual triflouroacetic acid is removed with ethyl acetate by azeotroping conditions. The final residue is purified over silica (hexanes/ethyl acetate 80:20) to afford 10.1 g (85% yield) of the desired product as a slightly yellow oil. 1H-NMR, (300 MHz, CDCl3): δ 1.23 (m, 3H), 2.41–2.54 (m, 1H), 2.82–3.06 (m, 2H), 3.61–3.73 (m, 1H), 3.82–3.98 (m, 1H), 4.06–4.25 (m, 1H), 4.61 (br s, 2H), 5.24–5.53 (m, 3H), 5.86–6.01 (m, 1H); MS (ESI): m/e=230.03 (M+H).

Workup

  1. customAfter the consumption of starting material
  2. customThe residual triflouroacetic acid is removed with ethyl acetate
  3. customby azeotroping conditions
  4. customThe final residue is purified over silica (hexanes/ethyl acetate 80:20)

Sources & evidence

ORD record
ord-39e47a6bd8e8422aa51971ae975ca22f
Source dataset
uspto-grants-2006_05
Patent number
US07041696B2

Reaction notes

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