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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407889Generated: October 30, 2026

Bromotrimethylsilane → HCID 53476318, compound

https://huagongshe.com/reaction/2407889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 86678285HCID 86678285—
SolventDichloromethaneHCID 6344—
ProductHCID 53476318HCID 53476318—

Reaction Steps

A solution of (6S,9R,13R)-9-amino-13-(dodecanoyloxy)-6-methyl-8,16-dioxo-4,15-dioxa-11-thia-7-azaheptacosylphosphonic acid diethyl ester (1 eq, from the previous step) in DCM (0.1 M) was added TMSBr (10 eq) and stirred at room temperature overnight. The reaction mixture was concentrated en vaccuo. The crude mixture was purified by reverse phase high performance liquid chromatography (HPLC) with C4 column eluting with a gradient of 40-80% MeCN/10 mM NH4OAc (95:5) in 10 mM NH4OAc (pH 9). The fractions containing the product were combined and lyophilized to give the desired product as a solid. 1H NMR (DMSO-d6): δ 7.97 (d, 1H), 5.09 (m, 1H), 4.27 (dd, 1H), 4.09 (dd, 1H), 3.86 (m, 1H), 3.20-3.43 (m, 5H), 2.59-2.85 (m, 4H), 2.24-2.27 (m, 4H), 1.62-1.69 (m, 2H), 1.23-1.51 (m, 38H), 1.14 (d, 3H), 0.83-0.88 (m, 6H). LRMS [M+H]=739.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08808703B2
Source datasetuspto-grants-2014_08
ORD IDord-f04b5b12fbba45f4b6afc1e3fc6ceaa9
Source noteuspto-grants-2014_08