HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895085Generated: October 30, 2026
Tetrahydrofuran → HCID 86588245, compound
https://huagongshe.com/reaction/895085
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | (3-Iodopropyl)trimethoxysilane | HCID 2759373 | — |
| Product | HCID 86588245 | HCID 86588245 | — |
Reaction Steps
To a 1.5 M solution of LDA.THF in cyclohexane (200.00 mL, 300.00 mmol) and THF (400 mL), cooled to −78° C. in a dry ice/acetone bath, t-butyl acetate (34.85 g, 300.00 mmol) was added dropwise over 15 min. After 1 h at −78° C., 3-iodopropyltrimethoxysilane (43.53 g, 150.00 mmol) was added dropwise over 15 min. The reaction mixture was allowed to stir at −78° C. for 1 h, sealed with a teflon stopper, and kept in a freezer at −15° C. for 3 days. The cold reaction mixture was vacuum filtered through silica gel (500 mL), eluted with 1:1 hexanes/THF (1000 mL), and concentrated to provide 60.10 g of a pale yellow oil. A quick distillation produced the volatile components, and 27.14 g of a colorless oil was recovered: bp 80-110° C. (0.7-1.0 mm). This material was purified by fractional distillation to provide 14.39 g (30%) of a colorless oil: bp 75-6° C. (0.06 mm); 1H NMR (CDCl3) δ 3.53 (s, OMe), 2.22 (t, CHcCO), 1.63 (quinet, CH2), 1.45 (m, CH2), 1.45 (s, tBuO), 1.31 (s, tBu), 0.62 (m, CH2Si).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06913865B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-47deac4e1bc24976b6a13b621ce9a4ba |
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| Source note | uspto-grants-2005_07 |
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