HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882144Generated: October 30, 2026
Hydrochloric Acid → 2-(((tert-Butyldimethylsilyl)oxy)methyl)acrylic acid
https://huagongshe.com/reaction/882144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Lithium 2-(hydroxymethyl)prop-2-enoate | HCID 89613527 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(((tert-Butyldimethylsilyl)oxy)methyl)acrylic acid | HCID 44604257 | — |
Reaction Steps
To lithium 2-(hydroxymethyl)prop-2-enoate (926 mg, 8.57 mmol) was added DMF (17.0 mL), HCl (1.07 mL, 4 M in dioxanes, 4.28 mmol) and imidazole (700 mg, 10.3 mmol), followed by TBS-Cl (2.84 g, 18.9 mmol) at 25° C. The reaction was stirred overnight, then quenched by pouring into a separatory funnel containing water. The aqueous layer was brought to pH˜3 with 1 N HCl and was extracted with ethyl acetate (×3). The organic layers were combined and dried with Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by chromatography using MPLC using 5-80% EtOAc/hexanes. The monoprotected product was collected and concentrated in vacuo to afford a clear oil. 1H NMR (600 MHz, DMSO-D6) δ 12.67 (s, 1H), 6.13 (s, 1H), 5.80 (s, 1H), 4.31 (s, 2H), 0.92 (s, 9H), 0.09 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993756B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-512b8cdb14a048e8b47cf13463230c96 |
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| Source note | uspto-grants-2015_03 |
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