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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945346Generated: November 1, 2026

1,1,3,3-Tetramethylguanidine → Methyl 2-(benzyloxycarbonylamino)-2-(1,4-dioxaspiro[4.5]decan-8-ylidene)acetate

https://huagongshe.com/reaction/1945346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantMethyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(benzyloxycarbonylamino)-2-(1,4-dioxaspiro[4.5]decan-8-ylidene)acetateHCID 1125696526.8%

Reaction Steps

A solution of 1,4-dioxaspiro[4.5]decan-8-one (15 g, 96 mmol) in EtOAc (150 mL) was added to a solution of methyl 2-(benzyloxycarbonylamino)-2-(dimethoxyphosphoryl)acetate (21.21 g, 64.0 mmol) in 1,1,3,3-tetramethylguanidine (10.45 mL, 83 mmol) and EtOAc (150 mL). The resulting solution was the stirred at ambient temperature for 72 h and then it was diluted with EtOAc (25 mL). The organic layer was washed with 1N HCl (75 mL), H2O (100 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated. The residue was purified via Biotage (5% to 25% EtOAc/Hexanes; 300 g column). The combined fractions containing the product were then concentrated under vacuum and the residue was re-crystallized from hexanes/EtOAc to give white crystals that corresponded to methyl 2-(benzyloxycarbonylamino)-2-(1,4-dioxaspiro[4.5]decan-8-ylidene)acetate (6.2 g) 1H NMR (400 MHz, CDCl3-d) δ ppm 7.30-7.44 (5H, m), 6.02 (1H, br. s.), 5.15 (2H, s), 3.97 (4H, s), 3.76 (3H, br. s.), 2.84-2.92 (2H, m), 2.47 (2H, t, J=6.40 Hz), 1.74-1.83 (4H, m). LC (Cond. OL1): Rt=2.89 min. LC/MS: Anal. Calcd. For [M+Na]+ C19H23NNaO6: 745.21; found: 745.47

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394968B2
Source datasetuspto-grants-2013_03
ORD IDord-df9471b5ecac44bf9766783e44fa90ab
Source noteuspto-grants-2013_03