HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407889Generated: October 30, 2026
Bromotrimethylsilane → HCID 53476318, compound
https://huagongshe.com/reaction/2407889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 86678285 | HCID 86678285 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53476318 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08808703B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-f04b5b12fbba45f4b6afc1e3fc6ceaa9 |
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| Source note | uspto-grants-2014_08 |
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