HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655104Generated: October 30, 2026
Sodium borohydride → HCID 66978202, compound
https://huagongshe.com/reaction/655104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66974043 | HCID 66974043 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66978202 | HCID 66978202 | 94.1% |
Reaction Steps
1,4-Dimethyl-bicyclo[3.2.1]octan-3-one (260 g, 1.7 mol, obtained as above in EXAMPLE III) was added to a suspension of sodium borohydride (NaBH4, 19 g, 0.5 mol) in isopropanol ((CH3)2CHOH, 400 mL), and refluxed for 30 minutes. The reaction mixture was cooled to room temperature, and quenched with acetone ((CH3)2CO) followed by acetic acid. The organic layer was separated and concentrated to provide crude 1,4-dimethyl-bicyclo[3.2.1]octan-3-ol (250 g, 1.6 mol), which was then added to a solution of acetic anhydride ((CH3CO)2O, 192 g, 1.9 mol) and Na2CO3 (4 g, 0.036 mol) and aged at 60° C. for 6 hours. The reaction mixture was subsequently washed with water followed by a Na2CO3 solution. Fractional distillation of the organic layer provided acetic acid 1,4-dimethyl-bicyclo[3.2.1]oct-3-yl ester (159 g) having a boiling point of 88° C. at a pressure of 15 mmHg
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071529B1 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-c37e9a41e2ab4fb5b322b202d6aa49c9 |
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| Source note | uspto-grants-2011_12 |
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