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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579487Generated: October 29, 2026

Tetrahydrofuran → Ethyl 2-(diphenylmethyleneamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate

https://huagongshe.com/reaction/579487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-(4-Bromobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11196311—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(diphenylmethyleneamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoateHCID 8666371264.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of N-(diphenylmethylene)glycine ethyl ester (8.24 g, 30.8 mmol) and 2-(4-bromobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8.92 g, 33.9 mmol) in freshly distilled THF (77 mL, 0.4 M) was cooled to −78° C. and treated with lithium bis(trimethylsilyl)amide (32.3 mL, 1.0 M in THF). Once the addition was complete, the reaction was warmed to 50° C. and heated for 8 h. After being complete by TLC, the reaction mixture was cooled to 0° C., diluted with ethyl acetate and washed successively with saturated aqueous NaHCO3 and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Rapid purification by MPLC (1-15% ethyl acetate in heptane with 0.5% triethylamine over 6 CV) gave ethyl 2-(diphenylmethyleneamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate as a colorless oil (8.9 g, 64%). Rf 0.40 (30% ethyl acetate in heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040703B2
Source datasetuspto-grants-2015_05
ORD IDord-9e22f3b5fdda46a881985e80fd92647c
Source noteuspto-grants-2015_05