Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805222Generated: October 27, 2026

Lithium Hexamethyldisilazide → (S)-4-{(Z)-2-[1-(4-iodo-phenyl)-cyclopropyl]-vinyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1805222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Iodophenyl)cyclopropanecarbaldehydeHCID 58256354—
Reactant(R)-4-(benzothiazole-2-sulfonylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 59173188—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-{(Z)-2-[1-(4-iodo-phenyl)-cyclopropyl]-vinyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6715168472.5%

Reaction Steps

To a stirred, cooled (0° C.) solution of 1-(4-iodo-phenyl)-cyclopropanecarbaldehyde (1.6 g) in tetrahydrofurane (40 ml) was added under an argon atmosphere (R)-4-(benzothiazole-2-sulfonylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (2.9 g) [CAS 1043499-96-2] followed by a 1 M solution of LiHMDS in THF (11.8 ml). After 1 h at 0° C. the cooling bath was removed and stirring was continued overnight. The mixture was quenched by the addition of sat. aqueous NH4Cl (50 ml) and H2O (50 ml) and extracted with EtOAc. The aqueous phase was back extracted with EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (SiO2; gradient: heptane->heptane/EtOAc 2:1) to give (S)-4-{(Z)-2-[1-(4-iodo-phenyl)-cyclopropyl]-vinyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (2.0 g) as light yellow solid. MS (ISP): 470.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354441B2
Source datasetuspto-grants-2013_01
ORD IDord-95c2be060b18479c80bf52e50557deb1
Source noteuspto-grants-2013_01