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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015459Generated: October 30, 2026

Sodium bis(trimethylsilyl)amide → Methyl 7-(N-(4-(1-(4-methoxybenzyloxy)hexyl)phenyl)acetamido)hept-5-ynoate

https://huagongshe.com/reaction/1015459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantMethyl 7-iodohept-5-ynoateHCID 10901527—
ReactantN-(4-(1-(4-methoxybenzyloxy)hexyl)phenyl)acetamideHCID 59728274—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 7-(N-(4-(1-(4-methoxybenzyloxy)hexyl)phenyl)acetamido)hept-5-ynoateHCID 5972826725.1%

Reaction Steps

Sodium bis(trimethylsilyl)amide (0.31 ml of a 1.0 M solution in THF, 0.31 mmol) was added to a solution of the aryl amide 103 (100 mg, 0.282 mmol) in THF (1.3 mL) at 0° C. After 15 min a solution of the methyl 7-iodohept-5-ynoate (90 mg, 0.338 mmol) in THF (0.3 mL) was added and the reaction was warmed room temperature. After stirring for 16 h the reaction was the quenched with saturated aqueous ammonium chloride and extracted with EtOAc. The organic portion was washed with brine, dried (MgSO4), filtered and the filtrate was concentrated in vacuo. Purification by FCC (silica gel, 3:2 hex/EtOAc) gave 35 mg (25%) of ester 104.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985767B2
Source datasetuspto-grants-2011_07
ORD IDord-ea88072c23bc40818eb850de148115f5
Source noteuspto-grants-2011_07