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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781310Generated: October 31, 2026

Trimethylsilyl iodide → HCID 54197837, compound

https://huagongshe.com/reaction/1781310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 19046189HCID 19046189—
ReactantHCID 54222219HCID 54222219—
ProductHCID 54197837HCID 5419783799.8%

Reaction Steps

tert-Butyl (4R)-3-2-aminoacetyl)-2-[(2RS)-5-norbornen-2-yl]-4-thiazolidinecarboxylate (mixture of isomers C and D) may be prepared in a manner similar to that described in Example 1B, but starting with 1.0 g of tert-butyl (4R)-3-(2-tert-butoxycarbonylaminoacetyl)-2-[(2RS)-5-norbornen-2-yl]-4-thiazolidinecarboxylate (mixture of isomers C and D) and 0.36 cm3 of iodotrimethylsilane. 0.77 g of tert-butyl (4R)-3-(2-aminoacetyl)-2-[(2RS)-5-norbornen-2-yl]-4-thiazolidinecarboxylate (mixture of isomers C and D) is thereby obtained in the form of a yellow oil, which is used in the subsequent syntheses without further treatment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633270
Source datasetuspto-grants-1997_05
ORD IDord-73543e7f76764526bdad67044d707af0
Source noteuspto-grants-1997_05