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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963103Generated: October 29, 2026

Sodium borohydride → HCID 66978202, compound

https://huagongshe.com/reaction/1963103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66974043HCID 66974043—
SolventIsopropanolHCID 3776—
ProductHCID 66978202HCID 6697820294.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415391B2
Source datasetuspto-grants-2013_04
ORD IDord-503d667ccb18495bac294fd9bbc6c4cd
Source noteuspto-grants-2013_04