HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483697Generated: October 29, 2026
Lithium tri-s-butylborohydride → 3-(3-Methoxy-3-methylbutyl)-5-methylcyclohexanol
https://huagongshe.com/reaction/483697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | 3-(3-Methoxy-3-methylbut-1-yl)-5-methylcyclohexan-1-one | HCID 14793994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-Methoxy-3-methylbutyl)-5-methylcyclohexanol | HCID 14793995 | — |
Reaction Steps
A solution of lithium tri-sec-butylborohydride (267 mL of a 1M solution in tetrahydrofuran, 0.27 mol) was added to a cooled (-65~C.) solution of 3-(3-methoxy-3-methylbutyl)-5 methylcyclohexan-1-one (48.6 g, 0.22 mol) dissolved in tetrahydrofuran (350 mL). The solution was stirred at 25~C. for 16 hours and was quenched by addition of sodium hydroxide (10% aqueous, 165 mL) followed by hydrogen peroxide (30% aqueous, 170 mL). Workup yielded 3-(3-methoxy-3-methylbutyl)-5-methyl cyclohexan-1-ol as a mixture of diastereoisomers (ratio 90.1:7.2:2.7), bp0.75 120-122~C. (40.7 g). This compound and mixtures of diastereomers possess strong, tenacious, sandalwoody, musky notes. NMR(CDCl3) δ 0.6 (q,1H), 0.9(d,3H), 1.0-1.1(m,2H), 1.1(s,6H), 1.2-1.3 (m,2H), 1.4-1.6(m,2H), 1.6-1.9(m,5H), 2.2(brs,1H), 3.2(s,3H), 4.1(m,1H). IR(neat) 2400, 2975, 2925, 1460, 1385, 1365, 1210, 1090, 1015 cm-1 ; MS(m/e) 43, 73, 93, 111, 149, 167, 182, 199, 200.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225608 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-0b95f658b12c44d78aa6524d8e706d72 |
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| Source note | uspto-grants-1993_07 |
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