Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379293Generated: October 29, 2026

Chlorotrimethylsilane → HCID 131720209, compound

https://huagongshe.com/reaction/1379293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 131720210HCID 131720210—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
ProductHCID 131720209HCID 13172020948.3%

Reaction Steps

To a stirred solution of 2'-deoxy-2'-methylthiocytidine (0.86 g, 3.15 mmol) in dry pyridine (20 ml) was added trimethylchlorosilane (2.0 ml, 15.75 mmol), and stirring continued for 15 min. Benzoyl chloride (2.18 ml, 18.9 mmol) was added to the solution followed by stirring for 2 hr. The mixture was then cooled in an ice-bath and MeOH (10 ml) was added. After 5 mins., NH4OH (20 ml, 30% aq.) was added and the mixture stirred for 30 min. The reaction mixture was then concentrated under vacuum and the residue purified by short silica gel (70 g) column chromatography. Elution with CH2Cl2 :MeOH (9:1, v/v), pooling of appropriate fractions and evaporation furnished the title compound (0.55 g, 46.6%) which crystallized from EtOH as needles, m.p. 193°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670633
Source datasetuspto-grants-1997_09
ORD IDord-dd0ebf93b17f4c858873407090d71944
Source noteuspto-grants-1997_09