HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422684Generated: October 30, 2026
Sodium Methoxide → HCID 178501328, compound
https://huagongshe.com/reaction/422684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178501333 | HCID 178501333 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178501328 | HCID 178501328 | — |
Reaction Steps
To a solution of trans-3-acetoxycyclobutanecarboxylic acid methyl ester (trans/cis=5:1) (4.70 g, 27.3 mmol) in dry methanol (45 mL) was added sodium methoxide (25 wt % solution in MeOH, 0.62 mL, 2.7 mmol), and the solution was stirred at ambient temperature. More NaOMe solution (0.31 mL, 2.4 mmol) was added after 1 h and 2 h, and stirring was continued overnight. Most of the methanol was evaporated, water was added (≈100 mL), and the mixture was extracted with CH2Cl2 (6×60 mL). The combined organic layers were washed with NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated (vacuum down to ≈40 mbar) to give the title compound as brown oil, trans/cis=5:1 based on 1H NMR. The material thus obtained was used without further purification. 1H NMR (CDCl3, 400 MHz) δ 2.17-2.27 (m, 2H), 2.54-2.64 (m, 2H), 3.00-3.09 (mc, 1H), 3.70 (s, 3H), 4.53-4.62 (mc, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101613B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-2e71cfbcbd894f8a8dabfb3ec35e40c7 |
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| Source note | uspto-grants-2012_01 |
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