HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660698Generated: October 31, 2026
Potassium borohydride → HCID 11738397, compound
https://huagongshe.com/reaction/1660698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 11278223 | HCID 11278223 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11738397 | HCID 11738397 | — |
Reaction Steps
To a solution of methyl ester 11 (2.8 g, 9.15 mmol) in HPLC MeOH (30 mL), cooled to −78° C., potassium borohydride (1.72 g, 32 mmol) was added in portions. The reaction mixture was stirred at −78° C. for 10 min, warmed to −20° C. for 30 min and then to 0° C. for 10 min. The reaction was quenched with acetic acid to pH 7 and extracted with CH2Cl2 (3×50 mL). The organic layer was washed with NaHCO3 (50 mL, sat), NaCl (50 mL, sat), dried (Na2SO4), filtered and evaporated. The alcohol 12 was obtained as a colorless oil (2.7 g, 98%) and used directly in the next step. 1H-NMR (500 MHz, CDCl3): 0.87 (d, J=6.7 Hz, 3H), 0.94 (d, J=6.7 Hz, 3H), 2.10-2.19 (m, 1H), 2.47 (dd, J=16.7 and 9.1 Hz), 2.58 (dd, J=16.7 and 2.9 Hz, 1H), 3.11-3.20 (m, 1H), 3.56-3.63 (m, 1H), 3.68 (s, 3H), 3.90-3.98 (m, 1H), 4.64 (d, J=7.9 Hz, 1H), 5.09 (s, 2H), 7.30-7.39 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030279B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-ffb8b69a5fca40b59e5a2be71ff0c4a6 |
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| Source note | uspto-grants-2011_10 |
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